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자료유형
학술저널
저자정보
Li Weijian (The Sixth Affiliated Hospital of Guangzhou Medical University) Chen Gaohuang (The Sixth Affiliated Hospital of Guangzhou Medical University) Feng Zhenyu (The Sixth Affiliated Hospital of Guangzhou Medical University) Zhu Baoyi (The Sixth Affiliated Hospital of Guangzhou Medical University) Zhou Lilin (The Sixth Affiliated Hospital of Guangzhou Medical University) Zhang Yuying (The Sixth Affiliated Hospital of Guangzhou Medical University) Mai Junyan (The Sixth Affiliated Hospital of Guangzhou Medical University) Jiang Chonghe (The Sixth Affiliated Hospital of Guangzhou Medical University) Zeng Jianwen (The Sixth Affiliated Hospital of Guangzhou Medical University)
저널정보
한국유전학회 Genes & Genomics Genes & Genomics Vol.43 No.12
발행연도
2021.12
수록면
1,413 - 1,421 (9page)
DOI
10.1007/s13258-021-01175-z

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Background Prostate cancer (PCa) is one of the most common malignancies in men. YTHDF1 may play an important role in promoting PCa progression, but there is no reports to date on YTHDF1 function in PCa. Objective This study explored whether YTHDF1 could regulate TRIM44 in PCa cells. Methods By querying the TCGA database, we evaluated YTHDF1 expression in PCa, the OS and DFS of YTHDF1, and the correlation between YTHDF1 and TRIM44 in PCa. We constructed vectors to interfere with YTHDF1 expression and overexpress TRIM44 to examine the role of YTHDF1 and TRIM44 in PCa cells. Diferentially expressed mRNAs were identifed by mRNA sequencing. The levels of YTHDF1, TRIM44, LGR4, SGTA, DDX20, and FZD8 were measured by qRT-PCR and WB was used to determine YTHDF1 and TRIM44 expression. A CCK-8 assay was used to assess cell proliferation. A Transwell chamber assay was used measure cell migration and invasion ability. Results YTHDF1 was highly expressed in both Pca tissues and cells. PCa patient prognosis with high YTHDF1 expression was relatively poor. Cell function experiments showed that inhibiting YTHDF1 expression decreased cell proliferation, migration, and invasion. RNA sequencing analysis revealed that YTHDF1 may promote PCa cell proliferation, migration, and invasion by modulating TRIM44 expression. Cell function experiments further verifed that YTHDF1 promoted PCa cell proliferation, migration, and invasion by regulating TRIM44. Conclusions YTHDF1 enhances PCa cell proliferation, migration, and invasion by regulating TRIM44.

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