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Metastatic Lymph Node 64 (MLN64) Expression in Gastric Cancer: The Clinical and Molecular Implications in Drug Resistance.

Authors :
XINYU LI, AMBER
JIANYUAN ZENG, JIMMY
KHAN, ELYAS
PING DOU, Q.
XINGUO ZHUANG
KE JI, EDISON
FIONA RUGE
MARTIN, TRACEY A.
SHUQIN JIA
JIANG, WEN G.
Source :
Cancer Genomics & Proteomics (1109-6535); Jan/Feb2024, Vol. 21 Issue 1, p30-40, 11p
Publication Year :
2024

Abstract

Background/Aim: Metastatic lymph node 64 (MLN64) is often co-amplified with ERBB2 (HER2) and plays a role in the progression of breast and prostate cancer. The present study explored the expression of MLN64 in clinical gastric cancer in association with the ERBB family and its impact on drug resistance in patients. Materials and Methods: Two independent gastric cancer cohorts (n=324; n=87) were used to explore the expression profile of MLN64 in conjunction with ERBB family members in clinical gastric cancer and its association with neoadjuvant chemotherapy responses. Gastric cancer AGS and HCG27 cells with MLN64 knockdown were generated to determine the function of MLN64 in cell behavioural changes. Results: Gastric tumor tissues expressed significantly higher levels of MLN64 compared with normal tissues (p<0.01); however, MLN64 alone was a weak prognostic indicator. An integrated coexpression of MLN64, ERBB4, and NRG4 was a significant factor in assessing overall survival in both cohorts. MLN64 was a profound indicator of patient response to neoadjuvant chemotherapy. In vitro studies indicated a significant contribution of MLN64 to the response of gastric cancer cells to chemodrugs and Her-2 inhibitors. MLN64 knockdown also contributed to the adhesion and migration and suggested a possible mechanism mediated by the interaction between MLN64 and ERBBs. Conclusion: MLN64 is an indicator of patient response to neoadjuvant chemotherapy in gastric cancer. Together with the expression pattern of ERBB4, MLN64 is a poor prognostic factor for patients with gastric cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11096535
Volume :
21
Issue :
1
Database :
Complementary Index
Journal :
Cancer Genomics & Proteomics (1109-6535)
Publication Type :
Academic Journal
Accession number :
174553446
Full Text :
https://doi.org/10.21873/cgp.20427