2014
DOI: 10.1016/j.ejso.2013.11.008
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MicroRNA-30a-3p inhibits tumor proliferation, invasiveness and metastasis and is downregulated in hepatocellular carcinoma

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Cited by 73 publications
(63 citation statements)
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“…Supporting our observations, almost the entire miR-30 family (miR-30a,b,c,d) was shown to be downregulated in metastatic RCC tissue21. MiR-30a-3p has been proven to have the ability to restore CDH1 expression in hepatocellular carcinoma22. Further, it was observed that hypoxia induces EMT in RCC cells through downregulation of miR-30c-5p, which leads to subsequent increase of Slug expression and repression of E-cadherin production23.…”
Section: Discussionsupporting
confidence: 77%
“…Supporting our observations, almost the entire miR-30 family (miR-30a,b,c,d) was shown to be downregulated in metastatic RCC tissue21. MiR-30a-3p has been proven to have the ability to restore CDH1 expression in hepatocellular carcinoma22. Further, it was observed that hypoxia induces EMT in RCC cells through downregulation of miR-30c-5p, which leads to subsequent increase of Slug expression and repression of E-cadherin production23.…”
Section: Discussionsupporting
confidence: 77%
“…It is likely that additional pathways regulated by miR-30s also contribute to the antitumor effects. Although overexpression of miR-30s in distant organs has no effect on primary tumor growth, interestingly, miR-30s have been reported as tumor suppressors that inhibit proliferation in pancreatic cancer (34), hepatocellular carcinoma (35), breast cancer (36), myeloma (37), and colorectal cancer (17). The miR-30 family is also implicated to inhibit epithelial-mesenchymal transition in prostate cancer cells (38), pancreatic cells (39), and hepatocytes (22).…”
Section: Discussionmentioning
confidence: 99%
“…By directly targeting metadherin (MTDH), miR-30a inhibited liver cancer cell proliferation and promoted apoptosis as a onco-suppressor through PTEN/ AKT pathway [98]. Further study demonstrated that miR-30a regulated HCC cellular proliferation, invasion and metastasis by a mechanism involving reduction of vimentin and MMP3 expression and restoration of E-cadherin expression [70]. …”
Section: Activities Of Mir-30a In Cancer Progressionmentioning
confidence: 99%
“…Levels of miR-30a were found to remarkably descend in most of cancer tissues compared with those in adjacent non-tumorous tissues, such as colorectal cancer [67, 68], hepatocellular carcinoma [69, 70], breast cancer [71], renal cell carcinoma [72], chondrosarcoma [73], ovarian papillary serous carcinoma [74], and anaplastic thyroid cancer [75]. Furthermore, miR-30a expression decreased in patients with shorter overall survival and disease-free survival time in patients with NSCLC [19] and urothelial carcinoma of bladder [76], consistent with the lower expression of miR-30a in tumor tissues compared to their non-tumor lung tissues.…”
Section: Expression and The Clinical Significance Of Mir-30a In Cancermentioning
confidence: 99%