Literature DB >> 34643945

Metagenomics and chemotherapy-induced nausea: A roadmap for future research.

Sylvia L Crowder1, Aasha I Hoogland1, Taylor L Welniak1, Elizabeth A LaFranchise2, Kristen M Carpenter3, Daneng Li4, Daniel M Rotroff5, Arshiya Mariam5, Christine M Pierce6, Stacy M Fischer7, Anita Y Kinney8, Thi Dong-Binh Tran9, Farzaneh Rastegari9,10, Donna L Berry11, Martine Extermann12, Richard D Kim13, Danielle B Tometich1, Jane C Figueiredo14, Jameel Muzaffar15, Shahla Bari16, Kea Turner1, George M Weinstock9, Heather S L Jim1.   

Abstract

Uncontrolled chemotherapy-induced nausea and vomiting can reduce patients' quality of life and may result in premature discontinuation of chemotherapy. Although nausea and vomiting are commonly grouped together, research has shown that antiemetics are clinically effective against chemotherapy-induced vomiting (CIV) but less so against chemotherapy-induced nausea (CIN). Nausea remains a problem for up to 68% of patients who are prescribed guideline-consistent antiemetics. Despite the high prevalence of CIN, relatively little is known regarding its etiology independent of CIV. This review summarizes a metagenomics approach to the study and treatment of CIN with the goal of encouraging future research. Metagenomics focuses on genetic risk factors and encompasses both human (ie, host) and gut microbial genetic variation. Little work to date has focused on metagenomics as a putative biological mechanism of CIN. Metagenomics has the potential to be a powerful tool in advancing scientific understanding of CIN by identifying new biological pathways and intervention targets. The investigation of metagenomics in the context of well-established demographic, clinical, and patient-reported risk factors may help to identify patients at risk and facilitate the prevention and management of CIN.
© 2021 American Cancer Society.

Entities:  

Keywords:  chemotherapy; metabolome; microbiome; nausea; prevention; symptoms

Mesh:

Substances:

Year:  2021        PMID: 34643945      PMCID: PMC8776572          DOI: 10.1002/cncr.33892

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  129 in total

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Journal:  Cancer Chemother Pharmacol       Date:  2015-01-09       Impact factor: 3.333

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7.  Improved anti-emetic efficacy of 5-HT3 receptor antagonists in cancer patients with genetic polymorphisms of ABCB1 (MDR1) drug transporter.

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