Evidence map›Paper›PMID 40734564›Full record

ArticleTechnology and health care : official journal of the European Society for Engineering and Medicine2025

LncRNA-TIL1H mediates targeted regulation of the drug-resistant gene MDR1 and RAD21 to promote immune resistance and accelerate osteosarcoma progression.

Qiu-Yang Lu, Mei-Ling Lan, Nan Dai, Kai Xiong, Yu Fu, Wei Liang

Expression of concernAbstract read
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Article in Technology and health care : official journal of the European Society for Engineering and Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 1 paper.

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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Qiu-Yang LuDepartment of Oncology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0005-2392-5529
Mei-Ling LanDepartment of Oncology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0001-8376-3868
Nan DaiCancer Center, Army Medical University Daping Hospital, Chongqing, China.ORCID 0009-0009-2858-0477
Kai XiongDepartment of Oncology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0006-0454-8139
Yu FuDepartment of Oncology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0006-2690-9601
Wei LiangDepartment of Oncology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0003-7865-9374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundTargeted regulation of drug-resistant gene expression through lncRNA has emerged as a novel research direction for overcoming immune resistance in osteosarcoma. However, the specific effects and regulatory mechanisms of lncRNA-TIL1H on immune resistance in osteosarcoma remain unclear.ObjectiveTo explore the mechanism by which lncRNA-TIL1H targets the regulation of the drug-resistant genes MDR1 and RAD21.MethodsClinical samples including osteosarcoma tissues and adjacent tissues were collected for qPCR and WB analysis of lncRNA-TIL1H expression as well as MDR1 and RAD21. Acquisition of drug-resistant osteosarcoma cells by cisplatin treatment MG-63/R. The cells were divided into four groups: MG-63, MG-63/R, si-NC-MG-63/R, and si-TIL1H-MG-63/R group. Cell proliferation and colony formation, and migration and invasion were detected by CCK-8, Transwell and scratch assays. In addition, the effects on osteosarcoma after interfering with lncRNA-TIL1H were further explored by the animal experiments, including HE staining and immunohistochemistry.ResultsThe expression of lncRNA-TIL1H and the drug-resistant genes MDR1 and RAD21 significantly increased in osteosarcoma. si-TIL1H effectively inhibited cell proliferation, invasion, migration and decreased the expression of drug-resistant genes in MG-63/R. Finally, the animal experiments revealed that si-lncRNA-TIL1H inhibited tumor proliferation.ConclusionThe expression of lncRNA-TIL1H in MG-63/R promotes the upregulation of drug-resistant genes MDR1 and RAD21, leading to the occurrence of immune resistance and accelerating osteosarcoma progression.

Indexed as

drug-resistantimmune resistancelncRNA-TIL1HMDR1OsteosarcomaRAD21

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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.