ER membrane protein complex subunit 6 (EMC6) is a novel tumor suppressor in gastric cancer
0
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
The endoplasmic reticulum (ER) membrane protein complex subunit 6 (EMC6) is a novel human autophagy-related molecule. Here, using tissue microarray and immunohistochemistry, we report that EMC6 protein is lost or reduced in glandular cells of patients with gastric adenocarcinoma, compared to normal stomach mucosa. Overexpression of EMC6 in gastric cancer cells inhibited cell growth, migration, invasion, and induced apoptosis and cell cycle arrest at S-phase. Further investigation suggested that EMC6 overexpression in BGC823 human adenocarcinoma gastric cancer cells reduced tumorigenicity in a xenograft model, demonstrating that EMC6 has the characteristics of a tumor suppressor. This is the first study to show that EMC6 induces cell death in gastric cancer cells. The molecular mechanism of how EMC6 functions as a tumor suppressor needs to be further explored.
Abstract
The endoplasmic reticulum (ER) membrane protein complex subunit 6 (EMC6) is a novel human autophagy-related molecule. Here, using tissue microarray and immunohistochemistry, we report that EMC6 protein is lost or reduced in glandular cells of patients with gastric adenocarcinoma, compared to normal stomach mucosa. Overexpression of EMC6 in gastric cancer cells inhibited cell growth, migration, invasion, and induced apoptosis and cell cycle arrest at S-phase. Further investigation suggested that EMC6 overexpression in BGC823 human adenocarcinoma gastric cancer cells reduced tumorigenicity in a xenograft model, demonstrating that EMC6 has the characteristics of a tumor suppressor. This is the first study to show that EMC6 induces cell death in gastric cancer cells. The molecular mechanism of how EMC6 functions as a tumor suppressor needs to be further explored.
참고문헌 (13)
- Li Y, "A novel ER-localized transmembrane protein, EMC6, interacts with RAB5A and regulates cell autophagy", Autophagy, 9, pp.150~163 (2013)
- Christianson JC, "Defining human ERAD networks through an integrative mapping strategy", Nat Cell Biol, 14, pp.93~105 (2012)
- Shen X, "EMC6", TMEM93 suppresses glioblastoma proliferation by modulating autophagy, 2016, pp.7, e2043~
- Richard M, "Biosynthesis of ionotropic acetylcholine receptors requires the evolutionarily conserved ER membrane complex", Proc Natl Acad Sci U S A, 110, pp.E1055~E1063 (2013)
- Szász AM, "Crossvalidation of survival associated biomarkers in gastric cancer using transcriptomic data of 1,065 patients", Oncotarget, 7, pp.49322~49333 (2016)
- Klionsky DJ, "Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)", Autophagy, 12, pp.1~222 (2016)
- Jonikas MC, "Comprehensive characterization of genes required for protein folding in the endoplasmic reticulum", Science, 323, pp.1693~1697 (2009)
- Ruggiano A, "Quality control: ER-associated degradation: protein quality control and beyond", J Cell Biol, 204, pp.869~879 (2014)
- Wideman JG, "The ubiquitous and ancient ER membrane protein complex (EMC): tether or not? Version 2", F1000Res 4, 624, ~ (2015)
- Lahiri S, "A conserved endoplasmic reticulum membrane protein complex (EMC) facilitates phospholipid transfer from the ER to mitochondria", PLoS Biol, 12, pp.e1001969~ (2014)
- Satoh T, "dPob", EMC is essential for biosynthesis of rhodopsin and other multi-pass membrane proteins in Drosophila photoreceptors, 2015, pp.4, e06306~
- Bagchi P, "EMC1-dependent stabilization drives membrane penetration of a partially destabilized non-enveloped virus", eLife, 5, pp.e21470~ (2016)
- Harel T, "Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy", Am J Hum Genet, 98, pp.562~570 (2016)
