دورية أكاديمية

Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers.

التفاصيل البيبلوغرافية
العنوان: Alternative Energy: Breaking Down the Diverse Metabolic Features of Lung Cancers.
المؤلفون: Cargill KR; Department of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States., Hasken WL; Department of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States., Gay CM; Department of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States., Byers LA; Department of Thoracic/Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
المصدر: Frontiers in oncology [Front Oncol] 2021 Oct 21; Vol. 11, pp. 757323. Date of Electronic Publication: 2021 Oct 21 (Print Publication: 2021).
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101568867 Publication Model: eCollection Cited Medium: Print ISSN: 2234-943X (Print) Linking ISSN: 2234943X NLM ISO Abbreviation: Front Oncol Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: [Lausanne : Frontiers Research Foundation]
مستخلص: Metabolic reprogramming is a hallmark of cancer initiation, progression, and relapse. From the initial observation that cancer cells preferentially ferment glucose to lactate, termed the Warburg effect, to emerging evidence indicating that metabolic heterogeneity and mitochondrial metabolism are also important for tumor growth, the complex mechanisms driving cancer metabolism remain vastly unknown. These unique shifts in metabolism must be further investigated in order to identify unique therapeutic targets for individuals afflicted by this aggressive disease. Although novel therapies have been developed to target metabolic vulnerabilities in a variety of cancer models, only limited efficacy has been achieved. In particular, lung cancer metabolism has remained relatively understudied and underutilized for the advancement of therapeutic strategies, however recent evidence suggests that lung cancers have unique metabolic preferences of their own. This review aims to provide an overview of essential metabolic mechanisms and potential therapeutic agents in order to increase evidence of targeted metabolic inhibition for the treatment of lung cancer, where novel therapeutics are desperately needed.
Competing Interests: CG serves in a consulting and advisory capacity for AstraZeneca, Kisoji Biotechnology, and Bristol Myers Squibb. CG is also a part of Speaker’s Bureau for AstraZeneca and Beigene. LB serves on advisory committees for AstraZeneca, AbbVie, GenMab, BergenBio, Pharma Mar SA, Sierra Oncology, Merck, Bristol Myers Squibb, Genentech, and Pfizer. LB also receives research support from AbbVie, AstraZeneca, GenMab, Sierra Oncology, Tolero Pharmaceuticals. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
(Copyright © 2021 Cargill, Hasken, Gay and Byers.)
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معلومات مُعتمدة: P30 CA016672 United States CA NCI NIH HHS; R01 CA207295 United States CA NCI NIH HHS; T32 CA009666 United States CA NCI NIH HHS
فهرسة مساهمة: Keywords: glycolysis (Warburg effect); lung cancer; metabolic inhibitors; metabolism; oxidative phosphorylation
تواريخ الأحداث: Date Created: 20211108 Latest Revision: 20240404
رمز التحديث: 20240404
مُعرف محوري في PubMed: PMC8566922
DOI: 10.3389/fonc.2021.757323
PMID: 34745994
قاعدة البيانات: MEDLINE