TY - JOUR
T1 - Sex differences in cancer mechanisms
AU - Rubin, Joshua B.
AU - Lagas, Joseph S.
AU - Broestl, Lauren
AU - Sponagel, Jasmin
AU - Rockwell, Nathan
AU - Rhee, Gina
AU - Rosen, Sarah F.
AU - Chen, Si
AU - Klein, Robyn S.
AU - Imoukhuede, Princess
AU - Luo, Jingqin
N1 - Funding Information:
Work in the Rubin Lab is supported by NIH, R01 CA174737 (JBR), The Children’s Discovery Institute of Washington University (JBR), Prayers for Maria Foundation (JBR), St Louis Children’s Hospital Foundation (JBR), Barnes-Jewish Hospital Foundation (JBR), Barnard Research Funds (JBR), Joshua’s Great Things Foundation (JBR). Work in the Klein lab is supported by NIH grants U19 AI083019 (RSK), R01 NS052632 (RSK), and R01 AI101400 (RSK) and National Society of Multiple Sclerosis (RSK). Work in the Imoukhuede Lab is supported by National Science Foundation 1653925 (PI) and the American Heart Association 16SDG26940002 (PI).
Publisher Copyright:
© 2020 The Author(s).
PY - 2020/4/15
Y1 - 2020/4/15
N2 - We now know that cancer is many different diseases, with great variation even within a single histological subtype. With the current emphasis on developing personalized approaches to cancer treatment, it is astonishing that we have not yet systematically incorporated the biology of sex differences into our paradigms for laboratory and clinical cancer research. While some sex differences in cancer arise through the actions of circulating sex hormones, other sex differences are independent of estrogen, testosterone, or progesterone levels. Instead, these differences are the result of sexual differentiation, a process that involves genetic and epigenetic mechanisms, in addition to acute sex hormone actions. Sexual differentiation begins with fertilization and continues beyond menopause. It affects virtually every body system, resulting in marked sex differences in such areas as growth, lifespan, metabolism, and immunity, all of which can impact on cancer progression, treatment response, and survival. These organismal level differences have correlates at the cellular level, and thus, males and females can fundamentally differ in their protections and vulnerabilities to cancer, from cellular transformation through all stages of progression, spread, and response to treatment. Our goal in this review is to cover some of the robust sex differences that exist in core cancer pathways and to make the case for inclusion of sex as a biological variable in all laboratory and clinical cancer research. We finish with a discussion of lab-and clinic-based experimental design that should be used when testing whether sex matters and the appropriate statistical models to apply in data analysis for rigorous evaluations of potential sex effects. It is our goal to facilitate the evaluation of sex differences in cancer in order to improve outcomes for all patients.
AB - We now know that cancer is many different diseases, with great variation even within a single histological subtype. With the current emphasis on developing personalized approaches to cancer treatment, it is astonishing that we have not yet systematically incorporated the biology of sex differences into our paradigms for laboratory and clinical cancer research. While some sex differences in cancer arise through the actions of circulating sex hormones, other sex differences are independent of estrogen, testosterone, or progesterone levels. Instead, these differences are the result of sexual differentiation, a process that involves genetic and epigenetic mechanisms, in addition to acute sex hormone actions. Sexual differentiation begins with fertilization and continues beyond menopause. It affects virtually every body system, resulting in marked sex differences in such areas as growth, lifespan, metabolism, and immunity, all of which can impact on cancer progression, treatment response, and survival. These organismal level differences have correlates at the cellular level, and thus, males and females can fundamentally differ in their protections and vulnerabilities to cancer, from cellular transformation through all stages of progression, spread, and response to treatment. Our goal in this review is to cover some of the robust sex differences that exist in core cancer pathways and to make the case for inclusion of sex as a biological variable in all laboratory and clinical cancer research. We finish with a discussion of lab-and clinic-based experimental design that should be used when testing whether sex matters and the appropriate statistical models to apply in data analysis for rigorous evaluations of potential sex effects. It is our goal to facilitate the evaluation of sex differences in cancer in order to improve outcomes for all patients.
KW - Angiogenesis
KW - Cancer
KW - Epigenetics
KW - Immunity
KW - Metabolism
KW - Senescence
KW - Sex differences
KW - Tumor Suppressor
KW - p53
UR - http://www.scopus.com/inward/record.url?scp=85083304995&partnerID=8YFLogxK
U2 - 10.1186/s13293-020-00291-x
DO - 10.1186/s13293-020-00291-x
M3 - Review article
C2 - 32295632
AN - SCOPUS:85083304995
SN - 2042-6410
VL - 11
JO - Biology of Sex Differences
JF - Biology of Sex Differences
IS - 1
M1 - 17
ER -