PO.PR02.02 · 预防研究

Primate comparative oncology reveal humans' unique cancer susceptibility

编号 7639 展板 26 时间 4/22 09:00–12:00 区域 Section 36 主讲 Zachary Compton, PhD
分会场 Cancer and Cancer Related Alterations, Detection Approaches, and Molecular Characterization
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作者与单位

Zachary Taylor Compton1, Walker Mellon2, Lisa M. Abegglen3, Tara Harrison4, Joshua D. Schiffman5, Amy M. Boddy6, Carlo C. Maley7

1University of Arizona Cancer Center, Tucson, AZ,2University of Arizona College of Medicine - Phoenix, Phoenix, AZ,3University of Utah Huntsman Cancer Institute, Salt Lake City, UT,4North Carolina State College of Veterinary Medicine, Raleigh, NC,5Peel Therapeutics, Inc, Salt Lake City, UT,6UCSF Medical Ctr., Goleta, CA,7Arizona State Univ. Biodesign Institute, Tempe, AZ

摘要 Abstract

Studying cancer from an evolutionary perspective can yield important theoretical and applied insights; however, little is known about the prevalence of cancer among non-human primates. Non-human primates are our closest living relatives, yet the primate lineage is phenotypically diverse, exhibiting wide variation in evolutionary and life-history characteristics. By integrating comparative phenotypic data with prevalence records of neoplastic disease, we assembled a dataset of 2,095 individuals from 36 species across nine primate families to examine cross-species cancer risk. Additionally, functional in vitro studies using isolated and cultured primary fibroblast cell lines from representative species show that resistance to cellular death correlates with certain life-history traits. Comparative phylogenetic modeling of human cancer risk, situated within the broader primate phylogeny, demonstrates a drastic reduction in cancer risk even among primates most closely related to humans (e.g., the great apes). Together, large-scale cancer prevalence records and functional assays provide valuable insights into the ecological and cellular dynamics of cancer in our closest living relatives-and in ourselves.
利益披露 Disclosure
Z. T. Compton, None.. W. Mellon, None.. T. Harrison, None.

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