Egyszerű keresés   |   Összetett keresés   |   Böngészés   |   Kosár   |   Súgó  


Részletek

A cikk állandó MOB linkje:
http://mob.gyemszi.hu/detailsperm.jsp?PERMID=163062
MOB:2024/1
Szerzők:Yan, Tingting; Lu, Guangxin; Shang, Rui; Hu, Junhua; Zhu, Chaobei
Tárgyszavak:GYOMOR DAGANATAI; SEJTEK; GÉNEK
Folyóirat:Physiology International - 2024. 111. évf. 1. sz.
[https://akjournals.com/view/journals/2060/2060-overview.xml]


  RACGAP1 drives proliferation, migration and invasion and suppresses autophagy of gastric cancer cells via inhibiting SIRT1/Mfn2 / Tingting Yan [et al.]
  Bibliogr.: p. 44-46. - Abstr. eng. - DOI: https://doi.org/10.1556/2060.2023.00235
  In: Physiology International. - ISSN 2498-602X, eISSN 2677-0164. - 2024. 111. évf. 1. sz., p. 35-46. : ill.


Objective: Gastric cancer is the most frequent gastrointestinal malignancy with a poor prognosis. Rac GTPase activation protein 1 (RACGAP1) is a novel tumor promotor, whose detailed effect on gastric cancer remains to be further elucidated. Hence, this study identifies the action of RACGAP1 on gastric cancer and investigates the potential mechanism. Methods: RACGAP1 expression in gastric cancer was analyzed based on the data of The Cancer Genome Atlas (TCGA) database. Cell proliferation was measured by CCK-8 and colony formation assay. Cell migration and invasion were evaluated by transwell assay. Cell apoptosis was assessed by flow cytometry. Cell autophagy was evaluated via determining LC3. Results: RACGAP1 presented at high level in gastric cancer cells. Overexpressed RACGAP1 potentiated gastric cancer cell proliferation, migration, and invasion. Besides, silenced RACGAP1 induced cell apoptosis and autophagy. Furthermore, RACGAP1 suppressed the expression of SIRT1 and Mfn2. Conclusion: RACGAP1 was overexpressed in gastric cancer. RACGAP1 potentiated aggressive behaviors of gastric cancer, and suppressed cell apoptosis and autophagy via modulating SIRT1/Mfn2. RACGAP1 may be a valuable target in the treatment of gastric cancer.  Kulcsszavak: RACGAP1, gastric cancer, invasion, autophagy, SIRT1/Mfn2