Fertility protection during chemotherapy treatment by boosting the NAD(P)+ metabolome

Author:

Ho Wing-Hong Jonathan,Marinova Maria B,Listijono Dave R,Bertoldo Michael J,Richani Dulama,Kim Lynn-Jee,Brown Amelia,Riepsamen Angelique H,Cabot Safaa,Frost Emily RORCID,Bustamante SoniaORCID,Zhong Ling,Selesniemi Kaisa,Wong Derek,Madawala Romanthi,Marchante MariaORCID,Goss Dale M,Li Catherine,Araki ToshiyukiORCID,Livingston David J,Turner Nigel,Sinclair David AORCID,Walters Kirsty A,Homer Hayden AORCID,Gilchrist Robert BORCID,Wu Lindsay EORCID

Abstract

AbstractChemotherapy induced ovarian failure and infertility is an important concern in female cancer patients of reproductive age or younger, and non-invasive, pharmacological approaches to maintain ovarian function are urgently needed. Given the role of reduced nicotinamide adenine dinucleotide phosphate (NADPH) as an essential cofactor for drug detoxification, we sought to test whether boosting the NAD(P)+ metabolome could protect ovarian function. We show that pharmacological or transgenic strategies to replenish the NAD+ metabolome ameliorates chemotherapy induced female infertility in mice, as measured by oocyte yield, follicle health, and functional breeding trials. Importantly, treatment of a triple-negative breast cancer mouse model with the NAD+ precursor nicotinamide mononucleotide (NMN) reduced tumour growth and did not impair the efficacy of chemotherapy drugs in vivo or in diverse cancer cell lines. Overall, these findings raise the possibility that NAD+ precursors could be a non-invasive strategy for maintaining ovarian function in cancer patients, with potential benefits in cancer therapy.

Funder

DHAC | National Health and Medical Research Council

American Federation for Aging Research

Publisher

Springer Science and Business Media LLC

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