Disease |
Disease |
Method |
Sample |
Expression pattern |
Dysfunction type |
Description |
PMID |
Source |
melanoma |
knockdown, affinity purification, mass spectrometry |
melanoma cells |
up-regulated |
expression |
SPRY4-IT1 knockdown may induce apoptosis via lipin 2-mediated alterations in lipid metabolism leading to cellular lipotoxicity. |
25344859 |
|
prostate cancer |
microarray, qPCR, knockdown etc. |
urine, cell lines (PC3, LNCaP) |
up-regulated |
expression |
We identified a group of differentially expressed long noncoding RNAs in prostate cancer cell lines and patient samples and further characterized six long noncoding RNAs (AK024556, XLOC_007697, LOC100287482, XLOC_005327, XLOC_008559, and XLOC_009911) in prostatic adenocarcinoma tissue samples and compared them with matched normal tissues. Interestingly, these markers were also successfully detetced in patient urine samples and were found to be up-regulated when compared with normal urine. |
25513185 |
Lnc2Cancer
|
breast cancer |
microarray, qPCR, Western blot, knockdown etc. |
breast cancer tissue, cell lines (MD-MB-231, MD-MB-435S, MCF-10A, MCF-7 etc.) |
up-regulated |
interaction |
SPRY4-IT1 expression was significantly upregulated in 48 breast cancer tumor tissues comparedwith normal tissues. Additionally, increased SPRY4-IT1 expression was found to be associated with a larger tumor size and an advanced pathological stage in breast cancer patients. SPRY4-IT1 is a novel prognostic biomarker and a potential therapeutic candidate for breast cancer. |
25742952 |
Lnc2Cancer
|
melanoma |
N/A |
N/A |
N/A |
expression |
The lncRNA, SPRY4-IT1, which is up-regulated in human melanomas compared to melanocytes and keratinocytes, affects cell dynamics, including increased rate of wound closure upon ectopic expression. |
22492512 |
LncRNADisease
|
melanoma |
N/A |
N/A |
N/A |
expression |
Another elegant study by Khaitan et al. utilized a non-coding RNA microarray approach to identify differentially regulated lncRNAs in melanoma cells and identified a 687 bp single exon lncRNA named SPRY4-IT1 which was highly up-regulated in melanoma patient samples and cell lines. |
24115003 |
LncRNADisease
|
esophageal squamous cell carcinoma |
qPCR etc. |
blood (plasma and serum) |
up-regulated |
expression |
Furthermore, plasma levels of POU3F3, HNF1A-AS1 and SPRY4-IT1 were significantly higher in ESCC patients compared with normal controls.By receiver operating characteristic curve (ROC) analysis, among the three lncRNAs investigated, plasma POU3F3 provided the highest diagnostic performance for detection of ESCC (the area under the ROC curve (AUC), 0.842. |
25608466 |
Lnc2Cancer
|
esophageal squamous cell carcinoma |
qPCR, knockdown etc. |
ESCC tissue, cell lines (KYSE-450, KYSE-510, KYSE-150 etc.) |
up-regulated |
expression |
Long?noncoding?RNA?SPRY4-IT1 is upregulated in esophageal squamous cell carcinoma and associated with poor prognosis. |
24810925 |
LncRNADisease Lnc2Cancer
|
clear cell renal cell carcinoma |
qPCR, knockdown etc. |
ccRCC tissue, cell lines (786-O, ACHN, Caki-1, Caki-2) |
up-regulated |
expression |
The relative level of SPRY4-IT1 was significantly higher in ccRCC tissues compared to the adjacent normal renal tissues. And higher expression of SPRY4-IT1 was found in renal cancer cell lines compared with the normal human proximal tubule epithelial cell line HK-2. The ccRCC patients with higher SPRY4-IT1 expression had an advanced clinical stage and poorer prognosis than those with lower SPRY4-IT1 expression. |
25337221 |
Lnc2Cancer
|
bladder cancer |
qPCR, knockdown etc. |
bladder cancer tissue, cell lines (J82, T24, SW780, SV-40 etc.) |
up-regulated |
expression |
SPRY4-IT1 levels were highly positively correlated with histological grade, tumor stage, and lymph node metastasis and reduced overall survival. A multivariate analysis showed that SPRY4-IT1 expression is an independent prognostic factor of overall survival in patients with UCB. |
25973088 |
Lnc2Cancer
|
melanoma |
qPCR, knockdown, FISH etc. |
melanoma tissue |
up-regulated |
N/A |
The melanoma-upregulated long noncoding RNA SPRY4-IT1 modulates apoptosis and invasion. |
21558391 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
qPCR, Western blot, knockdown etc. |
gastric cancer tissue, cell lines AGS, BGC-823, HGC-27, SGC-7901, MGC80-3, MKN-45) |
up-regulated |
N/A |
SPRY4-IT1 expression was elevated in GC tissues and cell lines |
25835973 |
LncRNADisease Lnc2Cancer
|
gastric cancer |
qPCR, Western blot, knockdown etc. |
gastric cancer tissue, cell lines (SGC7901, BGC823, MGC803, AGS, MKN45 etc.) |
down-regulated |
expression |
SPRY4-IT1 expression is decreased in gastric cancer tissues and associated with larger tumor size, advanced pathological stage, deeper depth of invasion and lymphatic metastasis. Patients with lower SPRY4-IT1 expression had a relatively poor prognosis. DNA methylation may be a key factor in controlling the SPRY4-IT1 expression. Furthermore, SPRY4-IT1 contributed to gastric cancer cells metastasis might partly via regulating epithelial-mesenchymal transition (EMT) process. |
26238992 |
Lnc2Cancer
|
glioma |
qPCR, Western blot, knockdown etc. |
glioma cell lines (U251, SF295) and the normal human astrocytes (NHA) |
up-regulated |
expression |
We examined for the first time the expression and role of SPRY4-IT1 in glioma cells. The results of our study showed that SPRY4-IT1 was up-regulated in human glioma tissues and cell lines. Knockdown of SPRY4-IT1 could inhibit glioma cell growth and migration. Moreover, knockdown of SPRY4-IT1 could inhibit epithelial-mesenchymal transition (EMT) phenotype in glioma cells. |
26464658 |
Lnc2Cancer
|
non-small-cell lung cancer |
qRT-PCR |
patients suffering from non-small-cell lung cancer (NSCLC) |
up-regulated |
expression |
N/A |
26448925 |
|
melanoma |
qRT-PCR, WB, knockdown |
severe preeclamptic placenta, trophoblast cells HTR-8/SVneo |
up-regulated |
expression |
SPRY4-IT1 knockdown enhanced the cell migration and proliferation, and reduced the response of cells to apoptosis. However, exogenous SPRY4-IT1 overexpression significantly decreased the cell migration and proliferation, while increased cell apoptosis. |
24223182 |
|
|