Evidence map›Paper›PMID 38151289›Full record

ArticleCancer genomics & proteomics

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

Amber Xinyu Li, Jimmy Jianyuan Zeng, Elyas Khan, Q Ping Dou, Xinguo Zhuang, Edison Ke Ji, Fiona Ruge, Tracey A Martin, Shuqin Jia, Wen G Jiang

Open access · diamondAbstract read
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Article in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Amber Xinyu LiCardiff University School of Medicine, Cardiff, U.K.
Jimmy Jianyuan ZengCardiff University School of Medicine, Cardiff, U.K.
Elyas KhanKarmanos Cancer Institute, Department of Oncology, School of Medicine, Wayne State University, Detroit, MI, U.S.A.
Q Ping DouCardiff University School of Medicine, Cardiff, U.K.
Xinguo ZhuangCardiff University School of Medicine, Cardiff, U.K.
Edison Ke JiGastrointestinal Cancer Centre, Peking University Cancer Hospital, Beijing, P.R. China.
Fiona RugeCardiff University School of Medicine, Cardiff, U.K.
Tracey A MartinCardiff University School of Medicine, Cardiff, U.K.
Shuqin JiaGastrointestinal Cancer Centre, Peking University Cancer Hospital, Beijing, P.R. China.
Wen G JiangCardiff University School of Medicine, Cardiff, U.K.; jiangw@cardiff.ac.uk.
Peking University · CNPeking University Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimMetastatic 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

methodsTwo 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.

resultsGastric 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 co-expression 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.

conclusionMLN64 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.

Indexed as

Stomach NeoplasmsCarrier ProteinsDrug ResistanceHumansLymph NodesMaleMembrane ProteinsPrognosisCarrier ProteinsMembrane ProteinsSTARD3 protein, humandrug responseERBB4gastric cancerMLN64NRGprognosissignallingSTARD3

Identifiers

PMID38151289
PMCPMC10756345
OpenAlexW4390267646

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.