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Nuclear Membrane Protein SUN5 Is Highly Expressed and Promotes Proliferation and Migration in Colorectal Cancer by Regulating the ERK Pathway.
Song, Xiaoyue; Li, Ruhong; Liu, Gang; Huang, Lihua; Li, Peng; Feng, Wanjiang; Gao, Qiujie; Xing, Xiaowei.
Afiliação
  • Song X; Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.
  • Li R; Department of Laboratory Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.
  • Liu G; Department of General Surgery, Yanan Hospital Affiliated to Kunming Medical University, Kunming 650051, China.
  • Huang L; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha 410078, China.
  • Li P; Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.
  • Feng W; Department of General Surgery, Yanan Hospital Affiliated to Kunming Medical University, Kunming 650051, China.
  • Gao Q; Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.
  • Xing X; Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, China.
Cancers (Basel) ; 14(21)2022 Oct 31.
Article em En | MEDLINE | ID: mdl-36358787
SUN5 was first identified as a nuclear envelope protein involved in spermatocyte division. We found that SUN5 was highly expressed in some cancers, but its function and mechanism in cancer development remain unclear. In the present study, we demonstrated that SUN5 was highly expressed in colorectal cancer (CRC) tissues and cells, as indicated by bioinformatics analysis, and SUN5 promoted cell proliferation and migration in vitro. Moreover, the overexpression of SUN5 upregulated phosphorylated ERK1/2 (pERK1/2), whereas the knockdown of SUN5 yielded the opposite results. PD0325901 decreased the level of pERK1/2 to inhibit cell proliferation and migration, which was partially reversed by SUN5 overexpression, indicating that drug resistance existed in patients with high SUN5 expression. The xenograft transplantation experiment showed that SUN5 accelerated tumor formation in vivo. Furthermore, we found that SUN5 regulated the ERK pathway via Nesprin2 mediation and promoted the nuclear translocation of pERK1/2 by interacting with Nup93. Thus, these findings indicated that highly expressed SUN5 promoted CRC proliferation and migration by regulating the ERK pathway, which may contribute to the clinical diagnosis and new treatment strategies for CRC.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article