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An omic and multidimensional spatial atlas from serial biopsies of an evolving metastatic breast cancer.

Authors :
Johnson BE
Creason AL
Stommel JM
Keck JM
Parmar S
Betts CB
Blucher A
Boniface C
Bucher E
Burlingame E
Camp T
Chin K
Eng J
Estabrook J
Feiler HS
Heskett MB
Hu Z
Kolodzie A
Kong BL
Labrie M
Lee J
Leyshock P
Mitri S
Patterson J
Riesterer JL
Sivagnanam S
Somers J
Sudar D
Thibault G
Weeder BR
Zheng C
Nan X
Thompson RF
Heiser LM
Spellman PT
Thomas G
Demir E
Chang YH
Coussens LM
Guimaraes AR
Corless C
Goecks J
Bergan R
Mitri Z
Mills GB
Gray JW
Source :
Cell reports. Medicine [Cell Rep Med] 2022 Feb 15; Vol. 3 (2), pp. 100525. Date of Electronic Publication: 2022 Feb 15 (Print Publication: 2022).
Publication Year :
2022

Abstract

Mechanisms of therapeutic resistance and vulnerability evolve in metastatic cancers as tumor cells and extrinsic microenvironmental influences change during treatment. To support the development of methods for identifying these mechanisms in individual people, here we present an omic and multidimensional spatial (OMS) atlas generated from four serial biopsies of an individual with metastatic breast cancer during 3.5 years of therapy. This resource links detailed, longitudinal clinical metadata that includes treatment times and doses, anatomic imaging, and blood-based response measurements to clinical and exploratory analyses, which includes comprehensive DNA, RNA, and protein profiles; images of multiplexed immunostaining; and 2- and 3-dimensional scanning electron micrographs. These data report aspects of heterogeneity and evolution of the cancer genome, signaling pathways, immune microenvironment, cellular composition and organization, and ultrastructure. We present illustrative examples of how integrative analyses of these data reveal potential mechanisms of response and resistance and suggest novel therapeutic vulnerabilities.<br />Competing Interests: D.S. is employed by Quantitative Imaging Systems. L.M.C. is a paid consultant for Cell Signaling Technologies, Shasqi, and AbbVie; received reagent and/or research support from Plexxikon, Pharmacyclics, Acerta Pharma, Deciphera Pharmaceuticals, Genentech, Roche Glycart AG, Syndax Pharmaceuticals, Innate Pharma, and NanoString Technologies; and is a member of the scientific advisory boards of Syndax Pharmaceuticals, Carisma Therapeutics, Zymeworks, Verseau Therapeutics, Cytomix Therapeutics, and Kineta. G.B.M. has licensed technologies to Myriad Genetics and NanoString; is on the SAB or is a consultant to Amphista, AstraZeneca, Chrysallis Biotechnology, GSK, ImmunoMET, Ionis, Lilly, PDX Pharmaceuticals, Signalchem Lifesciences, Symphogen, Tarveda, Turbine, and Zentalis Pharmaceuticals; and has stock/options/financial interests in Catena Pharmaceuticals, ImmunoMet, SignalChem, and Tarveda. J.W.G. has licensed technologies to Abbott Diagnostics, Zorro Bio, and PDX Pharmaceuticals; has ownership positions in Convergent Genomics, Health Technology Innovations, Zorro Bio, and PDX Pharmaceuticals; serves as a paid consultant to New Leaf Ventures; has received research support from Thermo Fisher Scientific (formerly FEI), Zeiss, Miltenyi Biotech, Cepheid (Danaher), Quantitative Imaging, Health Technology Innovations, and Micron Technologies; and owns stock in Abbott Diagnostics, AbbVie, Alphabet, Amazon, Amgen, Apple, General Electric, Gilead, Intel, Microsoft, Nvidia, and Zimmer Biomet.<br /> (© 2022 The Authors.)

Details

Language :
English
ISSN :
2666-3791
Volume :
3
Issue :
2
Database :
MEDLINE
Journal :
Cell reports. Medicine
Publication Type :
Academic Journal
Accession number :
35243422
Full Text :
https://doi.org/10.1016/j.xcrm.2022.100525