Disease |
Disease |
Method |
Sample |
Expression pattern |
Dysfunction type |
Description |
PMID |
Source |
colorectal cancer |
a case-control study |
N/A |
N/A |
N/A |
N/A |
27027436 |
|
gastric cancer |
AGS cells, knock out of H19 |
gastric cancer AGS cells |
down-regulated |
N/A |
H19 or miR-675 enhanced RUNX1 expression |
26931432 |
|
osteoarthritis |
cDNA array and quantitative RT-PCR |
OA and normal knee cartilage |
up-regulated |
interaction |
LncRNA H19 acts as a metabolic correlate in cartilage and cultured chondrocytes, while the miR-675 may indirectly influence COL2A1 levels. H19 may not only be an attractive marker for cell anabolism but also a potential target to stimulate cartilage recovery |
22527881 |
|
gallbladder cancer |
gallbladder cancer |
gallbladder cancer tissues and adjacent normal tissues |
up-regulated |
N/A |
The overexpression of H19 in GBC cells enhanced tumor invasion and promoted EMT |
27073719 |
|
bladder cancer |
ISH etc. |
bladder cancer tissue etc. |
differential expression |
expression |
The imprinted H19 gene is a marker of early recurrence in human bladder carcinoma. |
11193051 |
LncRNADisease Lnc2Cancer
|
gestational choriocarcinoma |
ISH etc. |
placenta tissue |
up-regulated |
expression |
Prominent expression of H19 was found in placental site trophoblastic tumor and gestational choriocarcinoma. |
8188082 |
LncRNADisease Lnc2Cancer
|
trophoblastic tumor |
ISH etc. |
placenta tissue |
up-regulated |
expression |
Prominent expression of H19 was found in placental site trophoblastic tumor and gestational choriocarcinoma. |
8188082 |
LncRNADisease Lnc2Cancer
|
laryngeal squamous cell carcinoma |
knockdown |
LSCC patients |
up-regulated |
N/A |
The inhibition of LSCC progression induced by H19 knockdown required the activity |
26872375 |
|
nasopharyngeal carcinoma |
knockdown |
NPC tissues |
up-regulated |
N/A |
H19 regulated EZH2 expression suppressing the activity of miR-630 |
27040767 |
|
hepatocelluar carcinoma |
microarray, qPCR etc. |
HCC tissue |
up-regulated |
expression |
We found that imbalances in levels of IGF2 and H19 transcripts were correlated with advanced tumor stage and poor outcome in HCC patients. |
15736456 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
microarray, qPCR etc. |
gastric cancer tissue, cell lines (GES-1, AGS, MGC-803, SGC-7901) |
up-regulated |
N/A |
As shown in Figure 2D, comparing with respective normal cell line, H19 was found highly expressed in stomach cancer cell lines (AGS, MGC-803 and SGC-7901) and hepatocellular carcinoma cell lines (SMMC-7721 and HepG2), while lowly expressed in lung cancer cell line (A549) and prostate cancer cell lines (Du-145 and PC-3). |
24063685 |
Lnc2Cancer
|
ovarian cancer |
microarray, qPCR etc. |
ovarian cancer tissue, cell lines (SKOV3, SKOV3.ip1 etc.) |
down-regulated |
N/A |
The qPCR results of seven lncRNAs (MALAT1, H19, UCA1, CCAT1, LOC645249, LOC100128881, and LOC100292680) were consistent with the deregulation found by microarray analysis, reflecting the reliability of the microarray data to some extent. |
24379988 |
Lnc2Cancer
|
gastric cardia adenocarcinoma |
microarray, qPCR etc. |
gastric cancer tissue |
up-regulated |
N/A |
H19 expression level was 4.97 to 13.58-fold higher in GCa samples than the mean level in paired non-cancerous tissues. Moreover, the expression levels of H19 were increased significantly in the tumors of patients with advanced clinical stage (p < 0.001) and larger tumor size ( p < 0.001). |
24414129 |
Lnc2Cancer
|
gastric cancer |
microarray, qPCR etc. |
gastric cancer tissue, cell lines (HCG-27, SGC-7901) |
up-regulated |
expression |
H19 and HOTAIR displayed significantly higher levels and the up-regulation of HOTAIR was associated with lymphatic metastasis and poor differentiation. |
26237576 |
Lnc2Cancer
|
hepatocelluar carcinoma |
microarray, qPCR, knockdown, ISH etc. |
cell lines (T24P, HepG2, Hep3B etc.) |
up-regulated |
N/A |
The H19 non-coding RNA is essential for human tumor growth. |
17786216 |
LncRNADisease Lnc2Cancer
|
bladder cancer |
microarray, qPCR, knockdown, ISH etc. |
cell lines (T24P etc.) |
up-regulated |
N/A |
The H19 non-coding RNA is essential for human tumor growth. |
17786216 |
LncRNADisease Lnc2Cancer
|
ovarian cancer |
microarray, qPCR, Western blot etc. |
cell lines (OVCAR-3, OV-90 and SK-OV-3) |
down-regulated |
interaction |
We find that overexpression of H1.3 decreases the growth rate and colony formation of OVCAR-3 cells. We identify histone H1.3 as a specific repressor for the noncoding oncogene H19. Overexpression of H1.3 suppresses H19 expression, and knockdown of H1.3 increases its expression in multiple ovarian epithelial cancer cell lines. Furthermore, we demonstrate that histone H1.3 overexpression leads to increased occupancy of H1.3 at the H19 regulator region encompassing the imprinting control region (ICR), concomitant with increased DNA methylation and reduced occupancy of the insulator protein CTCF at the ICR. Finally, we demonstrate that H1.3 overexpression and H19 knockdown synergistically decrease the growth rate of ovarian cancer cells |
25205099 |
Lnc2Cancer
|
glioma |
microarray, qPCR, Western blot, knockdown, Luciferase reporter assay etc. |
glioma tissue, cell lines (U87, U251 etc.) |
up-regulated |
regulation |
Long non-coding RNA H19 promotes glioma cell invasion by deriving miR-675. |
24466011 |
LncRNADisease Lnc2Cancer
|
colorectal cancer |
Multivariate analyses |
83 CRC patients |
up-regulated |
N/A |
overexpression of H19 promoted the proliferation of CRC cells; growth regulator |
26989025 |
|
choricarcinoma |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
type 2 diabetes mellitus |
N/A |
muscle of human subjects with type-2 diabetes and insulin resistant rodents. |
down-regulated |
expression |
H19 is significantly decreased in muscle of human subjects with type-2 diabetes and insulin resistant rodents. This decrease leads to increased bioavailability of let-7, causing diminished expression of let-7 targets, which is recapitulated in vitro where H19 depletion results in impaired insulin signaling and decreased glucose uptake. |
25399420 |
|
glioblastoma multiforme |
N/A |
GBM cell lines |
up-regulated |
N/A |
H19 in contributing to GBM malignancy |
26983719 |
|
cardiac hypertrophy |
N/A |
normal and diseased hearts |
up-regulated |
N/A |
overexpression of H19 reduced cell size both at baseline and in response to PE; knockdown of H19 induced cardiomyocyte hypertroph |
27084844 |
|
heart failure |
N/A |
normal and diseased hearts |
up-regulated |
N/A |
overexpression of H19 reduced cell size both at baseline and in response to PE; knockdown of H19 induced cardiomyocyte hypertroph |
27084844 |
|
myeloproliferative disease polycythaemia vera |
N/A |
N/A |
N/A |
expression |
Expression of the imprinted tumour-suppressor gene H19 is tightly regulated during normal haematopoiesis and is reduced in haematopoietic precursors of patients with the myeloproliferative disease polycythaemia vera. |
10640993 |
LncRNADisease
|
Marek's disease |
N/A |
N/A |
N/A |
mutation |
The mutant CVI/rpp38 was not only reactive with MAb H19 in IFA but also in immunoprecipitation. |
10696440 |
LncRNADisease
|
congenital hyperinsulinism |
N/A |
N/A |
N/A |
expression |
In agreement with the loss of the maternal chromosome, the level of expression of a maternally expressed tumor suppressor gene, H19, was greatly reduced compared to the level of expression of the paternally expressed growth promoter gene, IGF2. |
11395395 |
LncRNADisease
|
Beckwith-Wiedemann syndrome |
N/A |
N/A |
N/A |
epigenetics |
Mosaicism for 11p15 UPD and hypermethylation of the H19 gene in blood cells were associated with an increased risk of tumour. |
11436121 |
LncRNADisease
|
melanoma |
N/A |
N/A |
N/A |
expression |
The study of 4 sensitive and 2 resistant cell lines allowed the identification of 4 genes (RCC1, IFI16, hox2 and h19) preferentially transcribed in sensitive ((IFN-alpha therapy) cells and 2 (SHB and PKC-zeta) preferentially expressed in resistant cells. |
11437411 |
LncRNADisease
|
Beckwith-Wiedemann syndrome |
N/A |
N/A |
N/A |
epigenetics |
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. |
11813134 |
LncRNADisease
|
gestational trophoblastic diseases |
N/A |
N/A |
N/A |
expression |
LOI, deregulation of IGF2 promoters, and the altered expression levels of IGF2 and H19 genes might be associated with the progression of GTD. |
12648595 |
LncRNADisease
|
chronic myeloproliferative disorders |
N/A |
N/A |
N/A |
expression |
Reduced expression of H19 in bone marrow cells from chronic myeloproliferative disorders. |
12682647 |
LncRNADisease
|
biparental complete hydatidiform moles |
N/A |
N/A |
N/A |
epigenetics |
H19 is abnormally methylated on the maternal alleles in BiCHMs. |
12783848 |
LncRNADisease
|
Beckwith-Wiedemann syndrome |
N/A |
N/A |
N/A |
mutation |
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. |
15314640 |
LncRNADisease
|
colon cancer |
N/A |
N/A |
N/A |
expression |
DT-A was preferentially expressed in liver metastases after being transfected with H19 or IGF2-P3 promoter-driven DT-A expression plasmids, causing a very significant inhibition of tumor growth as a result of its cytotoxic effect. |
15521051 |
LncRNADisease
|
cancer |
N/A |
N/A |
N/A |
expression |
The human H19 gene is frequently overexpressed in myometrium and stroma during pathological endometrial proliferative events. |
15618002 |
LncRNADisease
|
hyperhomocysteinemia |
N/A |
N/A |
N/A |
epigenetics |
The effect of hyperhomocysteinemia on H19 DMD methylation was tissue-specific. hyperhomocysteinemia produces tissue-specific changes in H19 DMD methylation and increased vascular expression of H19 in adult mice. |
15899898 |
LncRNADisease
|
cancer |
N/A |
N/A |
N/A |
expression |
H19 expression was found in the hepatic metastases of 64 of 80 patients. High expression (higher staining grades) of H19 in the metastases was found in 43 of 80 patients. However, H19 expression status in the hepatic metastases did not correlate with either the length of time to development of metastasis or overall survival. |
16189152 |
LncRNADisease
|
Beckwith-Wiedemann syndrome |
N/A |
N/A |
N/A |
locus |
The H19 locus acts in vivo as a tumor suppressor. |
18719115 |
LncRNADisease
|
Silver-Russell syndrome |
N/A |
N/A |
N/A |
mutation |
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome |
19066168 |
LncRNADisease
|
pre-eclampsia |
N/A |
N/A |
N/A |
mutation |
LOI of H19 can be identified in pre-eclamptic placentas and is associated with maternal blood pressures, which implies the involvement of H19 gene LOI in the pathogenesis of pre-eclampsia and its potential relationship with the severity of the disease. |
19570415 |
LncRNADisease
|
melanoma |
N/A |
N/A |
N/A |
expression |
H19 RNA downregulation stimulated melanogenesis in melasma. |
19968822 |
LncRNADisease
|
infertility |
N/A |
N/A |
N/A |
expression |
H19 expression was lower in the infertility group as compared to the control group. |
20042264 |
LncRNADisease
|
growth restriction |
N/A |
N/A |
N/A |
epigenetics |
A loss of methylation at H19. |
20104244 |
LncRNADisease
|
glioblastoma |
N/A |
N/A |
N/A |
expression |
Another study performed in CD133+ and CD133- glioblastoma derived primary cell lines revealed levels of H19 expression that were relatively high and low, respectively. |
20380817 |
LncRNADisease
|
medulloblastoma |
N/A |
N/A |
N/A |
epigenetics |
A study of medulloblastomas and medulloblastoma cell lines showed partial loss of imprinting (LOI) and biallelic expression of H19. |
20380817 |
LncRNADisease
|
meningioma |
N/A |
N/A |
N/A |
epigenetics |
An examination of meningiomas (World Health Organization grades I-III) demonstrated more robustly that the imprinting status of H19 is perturbed with LOI in a significant number of these tumors. |
20380817 |
LncRNADisease
|
melanoma |
N/A |
N/A |
N/A |
mutation |
Although the IGF2 and H19 genotypes/haplotypes were not significantly associated with melanoma, two of the most severe cases (very early onset or multiple melanomas) showed to be heterozygous for both genes. |
20483645 |
LncRNADisease
|
Wiedemann-Beckwith syndrome |
N/A |
N/A |
N/A |
epigenetics |
Genetic analyses of the patient's blood showed hypermethylation at the H19 locus on chromosome 11p. |
21058226 |
LncRNADisease
|
Silver-Russell syndrome |
N/A |
N/A |
N/A |
epigenetics |
The major finding (~44%) is a hypomethylation of the imprinting control region 1 (ICR1) in 11p15.5 affecting the expression of H19 and IGF2. 4-10% of the patients carry a maternal UPD of chromosome 7 (UPD(7)mat). |
21150838 |
LncRNADisease
|
liver cancer |
N/A |
N/A |
N/A |
epigenetics |
H19 ICR showed loss-of-imprinting in two steps and allelic histone marker signature during tumorigenesis showed similarity with ES cells. |
21163252 |
LncRNADisease
|
Mullerian aplasia |
N/A |
N/A |
N/A |
epigenetics |
Methylation of H19 and its imprinted control region (H19 ICR1) in Mullerian aplasia. |
21458801 |
LncRNADisease
|
colon cancer |
N/A |
N/A |
N/A |
N/A |
Regional therapy with DTA-H19 vector suppresses growth of colon adenocarcinoma metastases in the rat liver. |
21874233 |
LncRNADisease
|
pheochromocytoma |
N/A |
N/A |
N/A |
mutation |
Tumor DNA from the index patient revealed loss of heterozygosity (LOH) at 11q23, causing loss of the wild-type paternal SDHD allele and LOH affecting maternal 11p15, including H19. |
21937622 |
LncRNADisease
|
atherosclerosis |
N/A |
N/A |
N/A |
epigenetics |
The most pronounced differences of atherosclerotic plaques in DNA methylation levels were registered for a site which is located in CpG-island of imprinted gene H19. |
21954592 |
LncRNADisease
|
breast cancer |
N/A |
N/A |
N/A |
mutation |
Different SNPs in LSP1 and H19 and in minor genes probably were associated with BC risk. |
21996731 |
LncRNADisease
|
adrenocortical carcinomas |
N/A |
N/A |
N/A |
epigenetics |
This disease has been associated with structural abnormalities at the 11p15 locus, which harbors the IGF2 gene as well as the genes coding for insulin, H19, and p57kip2. |
22019903 |
LncRNADisease
|
neural tube defects |
N/A |
N/A |
N/A |
epigenetics |
The methylation levels of H19 DMR1 in the NTD and control groups are 73.3%卤15.9 and 58.3%卤11.2, respectively. Hyper-methylation of the H19 DMR1 may be correlated with the occurrence of NTDs. |
22234160 |
LncRNADisease
|
obesity |
N/A |
N/A |
N/A |
epigenetics |
Insulin-like Growth Factor 2/H19 Methylation at Birth and Risk of Overweight and Obesity in Children. |
22341586 |
LncRNADisease
|
Wilms' tumor |
N/A |
N/A |
N/A |
epigenetics |
37% of patients with Wilms' tumor were H19 epimutations. |
22470196 |
LncRNADisease
|
bladder cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
breast cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
colon cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
esophageal squamous cell carcinoma |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
liver cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
lung cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting. Containing miRNA miR-675. |
22996375 |
LncRNADisease
|
tumor |
N/A |
N/A |
N/A |
epigenetics |
In recent years, we have extensively investigated the expression of the H19 gene in a number of human cancers and explored the role of H19 RNA in tumor development. |
23429271 |
LncRNADisease
|
tumor |
N/A |
N/A |
N/A |
expression |
H19, a lncRNA with oncogenic properties, is upregulated in a wide range of tumours. |
23660942 |
LncRNADisease
|
glioma |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
medulloblastoma |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
meningioma |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
neuroblastoma |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
pituitary adenoma |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
Prader-Willi syndrome |
N/A |
N/A |
N/A |
regulation |
Epigenetic deregulation of lncRNAs genes is associated with disease |
23791884 |
LncRNADisease
|
bladder cancer |
N/A |
N/A |
N/A |
expression |
Theseguilty by association studies have found numerous bladder-cancer associated lncRNAs |
24006935 |
LncRNADisease
|
hepatocelluar carcinoma |
N/A |
N/A |
N/A |
expression |
Dysregulation and functional roles of lncRNAs in HCC |
24183851 |
LncRNADisease
|
kidney cancer |
N/A |
N/A |
N/A |
regulation |
Tumour suppressor; tumour suppressor host |
24373479 |
LncRNADisease
|
bladder cancer |
N/A |
N/A |
N/A |
expression |
Prognostic marker low-risk marker Oncogene targeted therapy agent |
24373479 |
LncRNADisease
|
prostate cancer |
N/A |
N/A |
N/A |
expression |
Putative susceptibility and diagnostic marker |
24373479 |
LncRNADisease
|
bladder cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting breast, cervix, oesophagus prostate, endometrial, colon |
24499465 |
LncRNADisease
|
liver cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting breast, cervix, oesophagus prostate, endometrial, colon |
24499465 |
LncRNADisease
|
lung cancer |
N/A |
N/A |
N/A |
regulation |
Control of imprinting breast, cervix, oesophagus prostate, endometrial, colon |
24499465 |
LncRNADisease
|
tumor |
N/A |
N/A |
N/A |
regulation |
Oncofetal H19 RNA promotes tumor metastasis. |
24703882 |
LncRNADisease
|
hepatocelluar carcinoma |
N/A |
N/A |
N/A |
expression |
Overexpression of H19 was found in hepatocellular carcinoma.? |
24757675 |
LncRNADisease
|
gastric cancer |
N/A |
N/A |
N/A |
regulation |
Using real-time RT-PCR, flow cytometry, RNA immunoprecipitation and other methods, Yang et al confirmed that H19 expression in gastric cancer accelerated cell proliferation. |
24833871 |
LncRNADisease
|
coronary artery disease |
N/A |
N/A |
N/A |
N/A |
Re-expression of H19 has been observed in patients with atherosclerosis. Common polymorphisms of H19 are associated with the risk and severity of CAD in a Chinese population. |
25772106 |
LncRNADisease
|
Beckwith-Wiedemann syndrome |
N/A |
N/A |
N/A |
epigenetics |
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. |
7987305 |
LncRNADisease
|
cervical cancer |
N/A |
N/A |
N/A |
mutation |
High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. |
8570220 |
LncRNADisease
|
breast adenocarcinomas |
N/A |
breast adenocarcinoma stromal cells |
up-regulated |
expression |
An up-regulation of the h19 gene is significantly correlated with the tumor values and the presence of both estrogen and progesterone receptors |
9811352 |
|
bladder cancer |
PCR-RFLP etc. |
blood |
differential expression |
mutation |
A significantly decreased risk of bladder cancer was found for the rs2839698 TC genotype but not for CC homozygotes.The rs2839698 TC genotype was especially associated with a reduced risk of developing non-muscle-invasive disease. Borderline significantly |
18262338 |
LncRNADisease Lnc2Cancer
|
meningioma |
qPCR etc. |
meningioma tissue |
differential expression |
N/A |
In total, 24 meningiomas of WHO grade I, II and III were analysed. 15 meningiomas (63%) were informative for the ApaI polymorphism in the IGF2 gene. Monoallelic expression (MAE) for IGF2 was found in 11 out of 15 tumours (73%) which is in contrast to the lack of imprinting status of IGF2 in leptomeninges. Ten cases (42%) were heterozygous for the H19 gene and biallelic expression was found in 3 out of 10 meningiomas (30%). These results indicate that modulation of the imprinting status of IGF2 and H19 may play an important role for the development of meningiomas. |
10738131 |
Lnc2Cancer
|
colorectal cancer |
qPCR etc. |
CRC tissue |
up-regulated |
N/A |
LOI of IGF2 correlated strongly with biallelic hypermethylation of a core of five CpG sites in the insulator region of IGF2/H19, which is a known CTCF-binding element. As this methylation-dependent LOI was present in both tumors and normal colonic mucosa, it is possible that hypermethylation creates a field defect predisposing to cancer. |
11120891 |
Lnc2Cancer
|
germ cell tumor |
qPCR etc. |
germ cell tumor tissue |
differential expression |
epigenetics |
IGF2/H19 methylation status in GCTs might reflect preservation of the physiologic imprinting erasure in PGCs rather than a loss of imprinting in a sense that is accepted for somatic tumors. |
16001432 |
LncRNADisease Lnc2Cancer
|
breast cancer |
qPCR etc. |
cell lines (MCF10A, RPMI 1640, DMEM H21 etc.) |
up-regulated |
expression |
Down-regulation of H19 significantly decreases breast and lung cancer cell clonogenicity and anchorage-independent growth. In addition, c-Myc and H19 expression shows strong association in primary breast and lung carcinomas. |
16707459 |
LncRNADisease Lnc2Cancer
|
lung cancer |
qPCR etc. |
cell lines (MCF10A, RPMI 1640, DMEM H21 etc.) |
up-regulated |
expression |
Down-regulation of H19 significantly decreases breast and lung cancer cell clonogenicity and anchorage-independent growth. In addition, c-Myc and H19 expression shows strong association in primary breast and lung carcinomas. |
16707459 |
LncRNADisease Lnc2Cancer
|
breast cancer |
qPCR etc. |
breast cancer tissue |
differential expression |
mutation |
rs2107425 (C>T) near H19 was significantly associated with shorter metastasis-free survival in uni- and multi-variate analysis , with the more aggressive minor allele displaying a recessive trait. |
21748294 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
qPCR etc. |
gastric cancer tissue, cell lines (HGC27) |
up-regulated |
N/A |
Plasma H19 levels were significantly higher in patients than in healthy controls (p=0.029). Circulating lncRNAs can be detectable in plasma, and the detection of circulating lncRNAs may provide new complementary tumor markers for gastric cancer. |
23898077 |
Lnc2Cancer
|
hepatocelluar carcinoma |
qPCR etc. |
cell lines (SMMC-7721, HepG2) |
up-regulated |
N/A |
Comparing with respective normal cell line, H19 was found highly expressed in stomach cancer cell lines (AGS, MGC-803 and SGC-7901) and hepatocellular carcinoma cell lines (SMMC-7721 and HepG2), while lowly expressed in lung cancer cell line (A549) and prostate cancer cell lines (Du-145 and PC-3). |
24063685 |
Lnc2Cancer
|
prostate cancer |
qPCR etc. |
cell lines ((Du-145, PC-3) |
down-regulated |
N/A |
Comparing with respective normal cell line, H19 was found highly expressed in stomach cancer cell lines (AGS, MGC-803 and SGC-7901) and hepatocellular carcinoma cell lines (SMMC-7721 and HepG2), while lowly expressed in lung cancer cell line (A549) and prostate cancer cell lines (Du-145 and PC-3). |
24063685 |
Lnc2Cancer
|
lung cancer |
qPCR etc. |
cell lines (A549) |
down-regulated |
N/A |
Comparing with respective normal cell line, H19 was found highly expressed in stomach cancer cell lines (AGS, MGC-803 and SGC-7901) and hepatocellular carcinoma cell lines (SMMC-7721 and HepG2), while lowly expressed in lung cancer cell line (A549) and prostate cancer cell lines (Du-145 and PC-3). |
24063685 |
Lnc2Cancer
|
gastric cancer |
qPCR etc. |
gastric cancer tissue, cell lines(AGS, MKN45, 7901 etc.) |
up-regulated |
expression |
After validating in 20 pairs of tissues and plasma in training set, H19 was selected for further analysis in another 70 patients and 70 controls. Plasma level of H19 was significantly higher in GC patients compared with normal controls. |
26096073 |
Lnc2Cancer
|
liver cancer |
qPCR etc. |
hepatocellular carcinoma tissue |
up-regulated |
expression |
LncRNA profiling revealed that CD90+ cells were enriched in lncRNA H19, and released this through exosomes.Experiments of gain and loss of function of H19 showed that this LncRNA plays an important role in the exosome-mediated phenotype of endothelial cells. Moreover, we suggest the lncRNA H19 as a putative therapeutic target in hepatocellular carcinoma. |
26272696 |
Lnc2Cancer
|
medulloblastoma |
qPCR etc. |
fetal cerebella tissue, cell lines (MEB-MED, D283 etc.) |
differential expression |
expression |
Loss of imprinting of H19 occurred in 0 out of 4 informative fetal cerebella, 0 out of 1 informative adult cerebellum, 4 out of 8 informative medulloblastomas, and 1 out of 4 informative cell lines. The biallelic expression of H19 was only partial in two medulloblastomas, however, with one allele being significantly weaker than the other. |
8957451 |
Lnc2Cancer
|
breast cancer |
qPCR, ISH etc. |
MDA-MB-231 cell line |
up-regulated |
expression |
Overexpression of an ectopic H19 gene enhances the tumorigenic properties of breast cancer cells. |
12419837 |
LncRNADisease Lnc2Cancer
|
bladder cancer |
qPCR, ISH etc. |
cell lines (T24P, HT-1376 etc.) |
up-regulated |
N/A |
Bladder tumors may be successfully treated by intravesical instillation of the double promoter vector H19-DTA-P4-DTA. |
21162716 |
LncRNADisease Lnc2Cancer
|
breast cancer |
qPCR, knockdown etc. |
breast cancer tissue, cell lines (MCF7, T47D, BT20 etc.) |
up-regulated |
expression |
the transcript is stabilized in breast cancer cells and overexpressed in human breast tumors.91H expression is upregulated in breast cancer. |
18794369 |
LncRNADisease Lnc2Cancer
|
ovarian cancer |
qPCR, knockdown etc. |
cell lines (PC3, C2C12 etc.) |
up-regulated |
expression |
H19 RNA was detected in 90% of patients with OCAF (Ovarian cancer ascites fluid ) as determined by ISH. Intratumoral injection of DTA-H19 into ectopically developed tumors caused 40% inhibition of tumor growth. |
19656414 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
qPCR, knockdown etc. |
gastric cancer tissue, cell lines MGC-803, SGC-7901, GES-1) |
up-regulated |
regulation |
c-Myc-induced, long, noncoding H19 affects cell proliferation and predicts a poor prognosis in patients with gastric cancer. |
24671855 |
LncRNADisease Lnc2Cancer
|
esophageal squamous cell carcinoma |
qPCR, knockdown etc. |
ESCC tissue, cell lines (TE-1 ,Eca-109) |
down-regulated |
regulation |
Long non-coding RNA 91H contributes to the occurrence and progression of esophageal squamous cell carcinoma by inhibiting IGF2 expression. |
24706416 |
LncRNADisease Lnc2Cancer
|
colorectal cancer |
qPCR, knockdown etc. |
CRC tissue, cell lines ( HCT8, HT29, HCT116, SW620 etc.) |
up-regulated |
regulation |
91H was significantly overexpressed in cancerous tissue and CRC cell lines compared with adjacent normal tissue and a normal human intestinal epithelial cell line. Moreover, 91H overexpression was closely associated with distant metastasis and poor prognosis in patients with CRC, except for CNV of 91H. Multivariate analysis indicated that 91H expression was an independent prognostic indicator, as well as distant metastasis. 91H played an important role in the molecular etiology of CRC and might be regarded as a novel prognosis indicator in patients with CRC. |
25058480 |
Lnc2Cancer
|
skin cancer |
qPCR, lncRNA array analysis |
cultured mouse keratinocytes after deleting the vitamin D receptor (VDR) (∼90%) vs. control cells |
up-regulated |
expression |
Several well-known oncogenes, including H19, HOTTIP and Nespas, are significantly increased (6.3-1.8-fold), whereas tumor suppressors (Kcnq1ot1, lincRNA-p21) are decreased (up to 50-70%) in VDR deleted keratinocytes. |
24342142 |
|
bladder cancer |
qPCR, Luciferase reporter assay, in vitro knockdown, RIP etc. |
bladder cancer tissue, cell lines (RT4, RT112, DSH1, 253J, TCCSUP etc.) |
up-regulated |
regulation |
Upregulated H19 contributes to bladder cancer cell proliferation by regulating ID2 expression. |
23354591 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
qPCR, Luciferase reporter assays, in vitro knockdown, RIP etc. |
gastric cancer tissue,cell lines (AGS, MKN45, MGC803, SGC7901, GES-1 etc.) |
up-regulated |
N/A |
We demonstrated that H19 levels were markedly increased in gastric cancer cells and gastric cancer tissues compared with normal controls. Moreover, ectopic expression of H19 increased cell proliferation, whereas H19 siRNA treatment contributed to cell apoptosis in AGS cell line. We further verified that H19 was associated with p53, and that this association resulted in partial p53 inactivation. |
22776265 |
Lnc2Cancer
|
gastric cancer |
qPCR, Luciferase reporter assays, knockdown etc. |
gastric cancer tissue |
up-regulated |
interaction |
H19 expression was found to be inversely correlated to miR-141 expression in gastric cancer cells and tissues. H19 promotes malignancy including proliferation and invasion whereas miR-141 suppresses malignancy in human cancer cells. MiR-141 binds to H19 in a sequence specific manner, and suppresses H19 expression and functions including proliferation and invasion. MiR-141 could also regulate H19 target genes and miR-141 inhibitor restores H19 siRNA function, while H19 regulates miR-141 target gene ZEB1 |
26160158 |
Lnc2Cancer
|
non-small cell lung cancer |
qPCR, Luciferase reporter assays, knockdown, ChIP etc. |
NSCLC cell lines (A549, SPCA1) |
up-regulated |
interaction |
The higher expression of H19 was positively correlated with advanced tumor-node-metastasis (TNM) stage and tumor size. Multivariate analyses found that H19 expression could serve as an independent prognostic factor for overall survival of NSCLC. Moreover, chromatin immunoprecipitation (ChIP) assays revealed that H19 was a direct transcriptional target of c-Myc. And, knockdown of H19 significantly inhibited NSCLC cell proliferation both in vitro and in vivo. |
26482621 |
Lnc2Cancer
|
glioblastoma |
qPCR, Neurosphere Formation assay etc. |
glioblastoma tissue, cell lines (U87, U373) |
up-regulated |
expression |
H19 is significantly overexpressed in glioblastoma tissues, and the level of expression was associated with patient survival. In the subsequent investigations, the authors found that overexpression of H19 promotes glioblastoma cell invasion and angiogenesis in vitro. Interestingly, H19 was also significantly overexpressed in CD133+ glioblastoma cells, and overexpression of H19 was associated with increased neurosphere formation of glioblastoma cells. |
26274999 |
Lnc2Cancer
|
breast cancer |
qPCR, Northern blot etc. |
breast cancer tissue |
differential expression |
expression |
H19 RNA and insulin-like growth factor II mRNA were up-regulated significantly in non-neoplastic WAP-CRD-BP mammary tissue. |
14729626 |
LncRNADisease Lnc2Cancer
|
colon cancer |
qPCR, Northern blot, ISH etc. |
CRC tissue |
up-regulated |
locus |
Oncofetal H19-derived miR-675 regulates tumor suppressor RB in human colorectal cancer. |
19926638 |
LncRNADisease Lnc2Cancer
|
colorectal cancer |
qPCR, RFLP-PCR etc. |
CRC tissue |
up-regulated |
N/A |
The results of the present study suggest that LOI of IGF2 is important in the carcinogenesis of CRC. Hypomethylation of the sixth CTCF-binding site in the DMR of IGF2/H19 is linked to LOI and the common IGF2-H19 enhancer competition model for IGF2 imprinting does not apply to human CRC. |
22427002 |
Lnc2Cancer
|
bladder cancer |
qPCR, Western blot etc. |
bladder cancer tissue, cell lines (RT4, RT112, DSH1, 253J, TCCSUP etc.) |
up-regulated |
regulation |
Upregulated H19 contributes to bladder cancer cell proliferation by regulating ID2 expression. |
23399020 |
LncRNADisease Lnc2Cancer
|
chronic myeloid leukemia |
qPCR, Western blot etc. |
cell lines (K562) |
up-regulated |
N/A |
We observed that H19 was highly expressed in Bcr-Abl-expressing primary CML cells derived from 4 patients, and imatinib treatment greatly decreased the expression of H19 in these cells but not in normal control cells. Loss of either Bcr-Abl expression or Abl kinase activity caused decrease of c-Myc levels with simultaneously reduced levels of H19. Furthermore, we demonstrated that depletion of c-Myc alone in K562 cells significantly decreased the level of H19, suggesting that H19 is expressed in a c-Myc dependent manner in K562 leukemic cells. |
24685695 |
Lnc2Cancer
|
prostate cancer |
qPCR, Western blot etc. |
cell lines (P69, M12) |
down-regulated |
N/A |
In this study, we found that long non-coding RNA H19 (H19) and H19-derived microRNA-675 (miR-675) were significantly downregulated in the metastatic prostate cancer cell line M12 compared with the non-metastatic prostate epithelial cell line P69. Upregulation of H19 in P69 and PC3 cells significantly increased the level of miR-675 and repressed cell migration; however, ectopic expression of H19 in M12 cells could not increase the level of miR-675 and therefore had no effect on cell migration. |
24988946 |
Lnc2Cancer
|
bladder cancer |
qPCR, Western blot etc. |
bladder cancer tissue, cell lines (5637, UMUC-3, EJ) |
up-regulated |
interaction |
YAP1 and H19 expression levels were markedly elevated in bladder cancer tissues and cells, and H19 expression was found to be significantly associated with YAP1 expression. YAP1 and H19 were overexpressed were associated with poorer clinicopathologic prognosis. In addition, YAP1 was found to enhance H19 expression, whereas H19 had no significant effect on YAP1 expression in bladder cancer cells. |
26163939 |
Lnc2Cancer
|
gastric cancer |
qPCR, Western blot, knockdown etc. |
gastric cancer tissue, cell lines (AGS, MGC803 etc.) |
up-regulated |
N/A |
The expression levels of H19 and miR-675 in five gastric cancer cell lines were correlated with each other (r = 0.9910, P = 0.0315, data not shown). We next assessed the correlation of miR-675 and H19 expression in 24 human gastric cancer tissues. The expression of H19 and miR-675 in gastric cancer tissues was correlated with each other (r = 0.8214, P < 0.01). |
24388988 |
Lnc2Cancer
|
hepatocelluar carcinoma |
qPCR, Western blot, knockdown etc. |
cell lines (HepG2) |
up-regulated |
N/A |
We found that AFB1 could up-regulate the expression of H19 and promote cell growth and invasion by hepatocellular carcinoma HepG2 cells. AFB1 induced the expression of E2F1 and its knock-down could down-regulate H19 expression and suppress cell growth and invasion in hepatocellular carcinoma HepG2 cells. E2F1 over-expression could up-regulate H19 expression and promote cell growth and invasion, with binding to the H19 promoter being demonstrated by chromatin immunoprecipitation assays. |
24761865 |
Lnc2Cancer
|
pancreatic ductal adenocarcinoma |
qPCR, Western blot, knockdown etc. |
pancreatic cancer tissue, cell lines (PANC-1, SW1990, AsPC-1, BxPC-3, CFPAC-1 etc.) |
up-regulated |
N/A |
The levels of H19 was overexpressed in PDAC and was upregulated remarkably in primary tumors which subsequently metastasized, compared to those did not metastasis. H19 promoted PDAC cell invasion and migration. An important role of H19 in regulating metastasis of PDAC and provides some clues for elucidating the lncRNAmiRNA functional network in cancer. |
24920070 |
Lnc2Cancer
|
hepatocelluar carcinoma |
qPCR, Western blot, knockdown etc. |
cell lines (Huh-7, MHCC-97H, HepG2 etc.) |
up-regulated |
N/A |
The expression levels of LncRNAH19 and miR-675 were higher in MHCC-97H cells than in L02, Huh-7 and HepG2 cells. Transwell migration assay revealed that the miR-675 inhibitor and LncRNAH19siRNA could significantly increase the migration of HCC cells as compared with the control group. Transwell invasion assay demonstrated that the miR-675 inhibitor and LncRNAH19siRNA could significantly increase the invasion of HCC cells as compared with the control group. Inhibition of LncRNAH19 and miR-675 expression can promote migration and invasion of HCC cells via AKT/GSK-3β/Cdc25A signaling pathway. |
24939300 |
Lnc2Cancer
|
breast cancer |
qPCR, Western blot, knockdown etc. |
breast cancer tissue, cell lines (MCF-7, MDA-MB-231) |
up-regulated |
N/A |
H19 lncRNA mediates 17beta-estradiol-induced cell proliferation in MCF-7 breast cancer cells; H19 lncRNA was much higher in estrogen receptor (ER)-positive MCF-7 breast cancer cells than in ER-negative MDA-MB-231 cells |
25846769 |
LncRNADisease Lnc2Cancer
|
esophageal cancer |
qPCR, Western blot, knockdown etc. |
esophageal cancer tissue, cell lines (TE-1, TE-10, Eca-1, Eca-109, KYSE1170) |
up-regulated |
expression |
The expression of H19 was significantly increased and associated with tumor depth and metastasis in 133 EC samples. In addition, it was identified that an upregulation of H19 induced epithelial-to-mesenchymal transition. In conclusion, H19 has a significant role in the development of EC and may serve as a potential prognostic marker and therapeutic target for EC. |
26171017 |
Lnc2Cancer
|
ovarian cancer |
qPCR, Western blot, knockdown etc. |
ovarian cancer tissues and adjacent normal tissues, cell lines (SKOV3, OV90, TOV112D, ES2) |
up-regulated |
expression |
Our results demonstrated that that H19 silencing inhibited OV90 and SKOV3 OC cell proliferation in vitro. Further investigation into the mechanisms responsible for the growth inhibitory effects by H19 silencing revealed that its knockdown resulted in the induction of cell cycle arrest and apoptosis through certain cell cycle-related and apoptosis-related proteins |
26617715 |
Lnc2Cancer
|
colorectal cancer |
qPCR, Western blot, Luciferase reporter assay, RIP etc. |
CRC tissue, cell lines (SW620, HCT-116) |
up-regulated |
interaction |
We found that H19 was highly expressed in mesenchymal-like cancer cells and primary CRC tissues. H19 modulated the expression of multiple genes involved in EMT by acting as a competing endogenous RNA, which may build up the missing link between the regulatory miRNA network, EMT progression and accelerates in vivo and in vitro tumor growth. |
26068968 |
Lnc2Cancer
|
gastric cancer |
qPCR, Western blot, Luciferase reporter assays, knockdown etc. |
gastric cancer tissue, cell lines (SGC7901, MKN45, MKN-28 etc.) |
up-regulated |
expression |
Overexpression of?lncRNA?H19 enhances carcinogenesis and metastasis of gastric cancer. |
24810858 |
LncRNADisease Lnc2Cancer
|
bladder cancer |
qPCR, Western blot, Luciferase reporter assays, knockdown etc. |
bladder cancer tissues, cell lines (RT4, HT-1376, 5637, 253J, TCCSUP, T24,and J82) |
up-regulated |
interaction |
We found that miR-675 expression levels were remarkably increased in bladder cancer tissues as compared with adjacent noncancerous tissues or normal bladder tissue from health donors; moreover, enhanced miR-675 expression was also observed in bladder cancer cell lines. Ectopic expression of H19 significantly increased bladder cancer cell proliferation and miR-675 expression in vitro |
26198047 |
Lnc2Cancer
|
hepatocelluar carcinoma |
qPCR, Western bolt, Northern bolt, in vitro knockdown, RIP etc. |
HCC tissue, cell lines(SMMC7721, HCCLM3) |
down-regulated |
regulation |
Epigenetic activation of the MiR-200 family contributes to H19-mediated metastasis suppression in hepatocellular carcinoma. |
23222811 |
LncRNADisease Lnc2Cancer
|
clear cell renal cell carcinoma |
qRT-PCR, siRNA |
clear cell renal carcinoma (ccRCC) tissues and renal cancer cell lines |
up-regulated |
expression |
lncRNA H19 might be considered as a potential prognostic indicator and a target for gene therapy of ccRCC. |
25866221 |
|
gastric cancer |
real-time quantitative polymerase chain reaction (qPCR) assay |
gastric cancer (GC) tissues |
up-regulated |
expression |
H19 might serve as a promising biomarker for early detection and prognosis prediction of GC. |
26774144 |
|
breast cancer |
RNA CISH etc. |
breast cancer tissue |
up-regulated |
expression |
HOTAIR, H19 and KCNQ1OT1 had significantly higher expression levels in IBC than NA, and HOTAIR and H19 were both expressed more strongly in IBC than in DCIS tissues. |
26323944 |
Lnc2Cancer
|
non-small cell lung cancer |
RT-PCR, luciferase reporter assay, Chromosome immune coprecipitation (ChIP), disturbing and overexpressing the expression of H19, flow cytometry |
NSCLC tissues and cells, the adjacent tissues and normal cells |
up-regulated |
interaction |
lncRNA H19, which is induced by c-Myc, is up-regulated in NSCLC. H19 influences the mitotic progression of NSCLC cell lines. |
26722426 |
|
Wilms' tumor |
Southern blot, Northern blot etc. |
Wilms' tumor tissue |
differential expression |
epigenetics |
Gain of methylation at the H19 DMR is an early event in Wilms' tumorigenesis that is independent of chromosomal losses. |
16179496 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
stratified analyses |
gastric cancer samples |
up-regulated |
mutation |
We genotyped four lncRNA H19 single nucleotide polymorphisms (SNPs)(rs217727 C > T, rs2839698 C > T, rs3741216 A > T, rs3741219 T > C) in 500 GC patients and 500 healthy controls. These findings suggest that lncRNA H19 SNPs may contribute to susceptibility to GC. |
25944697 |
|
|