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Prognostic potential of METTL3 expression in patients with gastric cancer

Okugawa, Yoshinaga and Toiyama, Yuji and Yin, Chengzeng and Ruiya, Ma and Goel, Akul and Ichikawa, Takashi and Imaoka, Hiroki and Kitajima, Takahito and Shimura, Tadanobu and Kawamura, Mikio and Yasuda, Hiromi and Fujikawa, Hiroyuki and Yokoe, Takeshi and Mochiki, Ikuyo and Ohi, Masaki and Nakatani, Kaname (2022) Prognostic potential of METTL3 expression in patients with gastric cancer. Oncology Letters, 25 (2). Art. No. 64. ISSN 1792-1074. PMCID PMC9827465. doi:10.3892/ol.2022.13651. https://resolver.caltech.edu/CaltechAUTHORS:20230203-893210800.30

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Abstract

Methyltransferase‑like 3 (METTL3) is a crucial component of the m6A methyltransferase complex, which serves pivotal roles in tumor progression. The present study investigated the prognostic significance of METTL3 expression in gastric cancer (GC). The expression levels of METTL3 were assessed by immunohistochemistry in formalin‑fixed paraffin‑embedded (FFPE) tissue specimens from 158 patients with GC. Propensity score matching (PSM) analysis was performed to clarify its prognostic potential. METTL3 gene expression was also investigated in fresh frozen specimens from another independent cohort of 57 patients with GC to establish its clinical relevance. Knockdown of METTL3 by small interfering RNA transfection was performed to evaluate its function in vitro. METTL3 expression was significantly higher in cancerous tissues compared with in corresponding normal mucosa (P<0.0001), and high METTL3 expression was an independent prognostic factor for overall and disease‑free survival in the FFPE cohort of patients with GC. PSM analysis revealed that elevated METTL3 expression was significantly associated with poor survival outcomes, which was subsequently validated in another cohort of fresh frozen specimens. Knockdown of METTL3 inhibited proliferation, invasion, migration and anoikis resistance in GC cells. In conclusion, METTL3 expression may be used as a clinically feasible prognostic marker and could serve as a potential therapeutic target in patients with GC.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.3892/ol.2022.13651DOIArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/pmc9827465/PubMed CentralArticle
ORCID:
AuthorORCID
Okugawa, Yoshinaga0000-0002-0417-5559
Toiyama, Yuji0000-0003-1301-3268
Yin, Chengzeng0000-0002-1276-9904
Shimura, Tadanobu0000-0003-3760-8514
Mochiki, Ikuyo0000-0001-6361-5641
Nakatani, Kaname0000-0001-6709-541X
Additional Information:This work was supported in part by Grants-in-Aid for Scientific Research (grant nos. 18K08566, 18K08700, 18K08674, 18K08591 and 20K09004) from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
Funders:
Funding AgencyGrant Number
Ministry of Education, Culture, Sports, Science and Technology (MEXT)18K08566
Ministry of Education, Culture, Sports, Science and Technology (MEXT)18K08700
Ministry of Education, Culture, Sports, Science and Technology (MEXT)18K08674
Ministry of Education, Culture, Sports, Science and Technology (MEXT)18K08591
Ministry of Education, Culture, Sports, Science and Technology (MEXT)20K09004
Issue or Number:2
PubMed Central ID:PMC9827465
DOI:10.3892/ol.2022.13651
Record Number:CaltechAUTHORS:20230203-893210800.30
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20230203-893210800.30
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:119024
Collection:CaltechAUTHORS
Deposited By: Research Services Depository
Deposited On:24 Feb 2023 20:58
Last Modified:24 Feb 2023 20:58

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