Evidence map›Paper›PMID 30568499›Full record

ArticleCancer management and research2018

Identification of mTOR inhibitor-resistant genes in cutaneous squamous cell carcinoma.

Seong-Lan Yu, Dong Chul Lee, Seung Woo Baek, Do Yeun Cho, Jong Gwon Choi, JaeKu Kang

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Article in Cancer management and research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Seong-Lan YuMyunggok Medical Research Institute, College of Medicine, Konyang University, Daejeon, Republic of Korea, jaeku@konyang.ac.kr.
Dong Chul LeeBiotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Seung Woo BaekDepartment of Oncology-Hematology, Konyang University Hospital, Daejeon, Republic of Korea, jabuss@naver.com.
Do Yeun ChoDepartment of Oncology-Hematology, Konyang University Hospital, Daejeon, Republic of Korea, jabuss@naver.com.
Jong Gwon ChoiDepartment of Oncology-Hematology, Konyang University Hospital, Daejeon, Republic of Korea, jabuss@naver.com.
JaeKu KangMyunggok Medical Research Institute, College of Medicine, Konyang University, Daejeon, Republic of Korea, jaeku@konyang.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe PI3K/AKT/mTOR pathway is frequently activated in various squamous cell carcinomas (SCCs). Although mTOR inhibitors are suggested as effective treatments in immunosuppressed patients with metastatic SCC, they are still not proven to be favorable in treating skin SCC patients not undergoing immunosuppressive therapy. Moreover, the exact mechanism of the mTOR signaling pathway in SCC has not yet been identified. In this study, we aimed to determine the genes associated with mTOR inhibitors in skin SCC. MATERIALS AND

methodsThe identification of cell viability according to concentration of everolimus and Western blot was done. To analyze the global gene expression profiles, A431 and HSC-1 cells were treated with dimethyl sulfoxide (DMSO) or 100 nM of everolimus for 72 hours. Furthermore, differentially expressed genes (DEGs) were identified using Affymetrix analysis. To identify the gene network associated with everolimus resistance in SCC cells, pathway analysis was performed using the Ingenuity Pathway Analysis (IPA) tool.

resultsThe effects of cell death with respect to the mTOR inhibitor concentration were observed in the HSC-1 cell line; however, the mTOR inhibitor did not show effective cytotoxic activity in the A431 cell line. p-mTOR concentration also diminished with respect to everolimus concentrations in the HSC-1 cell line. Moreover, the microarray results showed that the

conclusionWe identified mTOR inhibitor resistance genes, and our findings may help select therapeutic targets in skin SCC.

Indexed as

CCND1 genegene profilingmTOR inhibitorsquamous cell carcinoma

Identifiers

PMID30568499
PMCPMC6267733

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