Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy

Author:

Davoli Teresa1,Uno Hajime2,Wooten Eric C.1,Elledge Stephen J.1

Affiliation:

1. Howard Hughes Medical Institute, Department of Genetics, Harvard Medical School, Division of Genetics, Brigham and Women’s Hospital, Boston, MA 02115, USA.

2. Dana-Farber Cancer Institute, Boston, MA 02215–5450, USA.

Abstract

Chromosomal chaos and tumor immunity Cancer immunotherapy produces durable clinical responses in only a subset of patients. Identification of tumor characteristics that correlate with responses could lead to predictive biomarkers and shed light on causal mechanisms. Davoli et al. found that human tumors with extensive aneuploidy—i.e., that display a highly abnormal number of chromosomes and chromosomal segments—express fewer markers of the immune cells responsible for tumor destruction. In a retrospective analysis of clinical trial data, they found that melanoma patients with highly aneuploid tumors were less likely to benefit from immune checkpoint blockade therapy than patients whose tumors had a more normal karyotype. Thus, aneuploidy appears to enhance the ability of tumors to evade the immune system. Science , this issue p. 10.1126/science.aaf8399

Funder

Department of Defense Breast Cancer Innovator Award

The Ludwig Foundation

NIH

NIH Pathway to Independence Award

Howard Hughes Medical Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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