<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>38(9)</volume><submitter>Zhong Y</submitter><pubmed_abstract>Ovarian cancer (OC) is the leading cause of death among women with gynecologic malignant diseases, however, the molecular mechanism of ovarian cancer is not well defined. Previous studies have found that RNA binding protein Lin28A is a key factor of maintain the pluripotency of stem cells, and it is positively correlated with the degree of several cancers (breast, prostate, liver cancer, etc). Our previous study shows that Lin28A is highly expressed in OC tissues and is involved in the regulation of OC cell biological behavior. In this study, we confirmed that high expression of Lin28A promoted the survival, invasion, metastasis, and inhibited the apoptosis of OC cells. Lin28A interacts with Rho associated coiled-coil containing protein kinase2 (ROCK2) but not ROCK1 and upregulates the exp</pubmed_abstract><journal>Oncogene</journal><pagination>1381-1397</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6372474</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The interaction of Lin28A/Rho associated coiled-coil containing protein kinase2 accelerates the malignancy of ovarian cancer.</pubmed_title><pmcid>PMC6372474</pmcid><pubmed_authors>Cao L</pubmed_authors><pubmed_authors>Zhou M</pubmed_authors><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Peng S</pubmed_authors><pubmed_authors>Zhong Y</pubmed_authors><pubmed_authors>Xiong W</pubmed_authors><pubmed_authors>Shuai C</pubmed_authors><pubmed_authors>Wei P</pubmed_authors><pubmed_authors>He S</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Ma H</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Yang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The interaction of Lin28A/Rho associated coiled-coil containing protein kinase2 accelerates the malignancy of ovarian cancer.</name><description>Ovarian cancer (OC) is the leading cause of death among women with gynecologic malignant diseases, however, the molecular mechanism of ovarian cancer is not well defined. Previous studies have found that RNA binding protein Lin28A is a key factor of maintain the pluripotency of stem cells, and it is positively correlated with the degree of several cancers (breast, prostate, liver cancer, etc). Our previous study shows that Lin28A is highly expressed in OC tissues and is involved in the regulation of OC cell biological behavior. In this study, we confirmed that high expression of Lin28A promoted the survival, invasion, metastasis, and inhibited the apoptosis of OC cells. Lin28A interacts with Rho associated coiled-coil containing protein kinase2 (ROCK2) but not ROCK1 and upregulates the exp</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2026-05-03T02:06:19.583Z</modification><creation>2025-05-29T19:55:17.29Z</creation></dates><accession>S-EPMC6372474</accession><cross_references><pubmed>30266988</pubmed><doi>10.1038/s41388-018-0512-9</doi></cross_references></HashMap>