Evidence map›Paper›PMID 38850316›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2024

TMEM205 induces TAM/M2 polarization to promote cisplatin resistance in gastric cancer.

Qiang Fu, Xuwei Wu, Zhongqi Lu, Ying Chang, Quanxin Jin, Tiefeng Jin, Meihua Zhang

Abstract read
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

15 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qiang Fu *Department of Ultrasound Medicine, Affiliated Hospital of Yanbian University, Yanji, 133000, Jilin, China.
Xuwei Wu *Department of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Zhongqi LuDepartment of Ultrasound Medicine, Affiliated Hospital of Yanbian University, Yanji, 133000, Jilin, China.
Ying ChangDepartment of Ultrasound Medicine, Affiliated Hospital of Yanbian University, Yanji, 133000, Jilin, China.
Quanxin JinDepartment of Immunology and Pathogenic Biology, Yanbian University Medical College, Yanji, China.
Tiefeng JinDepartment of Pathology and Cancer Research Center, Yanbian University Medical College, Yanji, 133002, China.
Meihua ZhangDepartment of Health Examination Centre, Yanbian University Hospital, Yanji, 133002, China. zhangmeihua@ybu.edu.cn.ORCID 0000-0003-0631-7933

Funding

Jilin Provincial Scientific and Technological Development Program YDZJ202201ZYTS131Jilin Provincial Scientific and Technological Development Program YDZJ202201ZYTS179National Natural Science Foundation of China 81960554
6 · The paper itself

Abstract

Cisplatin (DDP) is a basic chemotherapy drug for gastric cancer (GC). With the increase of DDP drug concentration in clinical treatment, cancer cells gradually became resistant. Therefore, it is necessary to find effective therapeutic targets to enhance the sensitivity of GC to DDP. Studies have shown that Transmembrane protein 205 (TMEM205) is overexpressed in DDP-resistant human epidermoid carcinoma cells and correlates with drug resistance, and database analyses show that TMEM 205 is also overexpressed in GC, but its role in cisplatin-resistant gastric cancer remains unclear. In this study, we chose a variety of experiments in vivo and vitro, aiming to investigate the role of TMEM 205 in cisplatin resistance in gastric cancer. The results showed that TMEM 205 promoted proliferation, stemness, epithelial-mesenchymal transition (EMT), migration and angiogenesis of gastric cancer cells through activation of the Wnt/β-catenin signaling pathway. In addition, TMEM205 promotes GC progression by inducing M2 polarization of tumor-associated macrophages (TAMs). These results suggest that TMEM205 may be an effective target to regulate the sensitivity of GC to DDP, providing a new therapeutic direction for clinical treatment.

Indexed as

Antineoplastic AgentsCell ProliferationCisplatinDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionMembrane ProteinsStomach NeoplasmsAnimalsAntigens, CDCell Line, TumorCell MovementHumansMiceMice, Inbred BALB CMice, NudeTumor-Associated MacrophagesAntigens, CDAntineoplastic AgentsCisplatinMembrane ProteinsCisplatin resistanceGastric cancerTransmembrane protein 205Tumor-associated macrophagesWnt/β-catenin

Identifiers

PMID38850316
PMCPMC11335886

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.