Andi Cani
Hematology and Oncology, Internal Medicine
Rogel Cancer Center, #7130, 1500 E. Medical Center Dr.
Ann Arbor, Michigan 48109
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About
Dr. Andi Cani, PhD, is an early-career research faculty member in the Breast Oncology Group of the Division of Hematology and Oncolgy at the Department of Internal Medicine, University of Michigan Medical School. His primary research interest is to investigate cancer molecular evolution by liquid biopsies in order to elucidate the mechanisms of response and resistance to therapies with the goal of enabling real-time adjustment of traditional, precision, and immunotherapies with improved outcomes. Dr. Cani's training and semi-independent work has been funded by internal, NIH, and foundation grants resulting in numerous and high-impact publications including 33 peer-reviewed articles and an H-index of 21.
Qualifications
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Postdoctoral Research FellowUniversity of Michigan–Ann Arbor, Hematology and Oncology, Internal Medicine, Ann Arbor, Michigan, 48109, United States
2020 - 2023
Postdoctoral Fellowship
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PhD, Molecular and Cellular PathologyUniversity of Michigan–Ann Arbor, Department of Pathology, Ann Arbor, Michigan, 48109, United States
2015 - 2020
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MS, Biochemistry and Molecular BiologyWayne State University, Biochemistry and Molecular Biology, School of Medicine, Detroit, Michigan, 48201, United States
2011 - 2013
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NA, Completed M1 and M2 year of MD DegreeRoss University School of Medicine, Bridgetown, Barbados
2008 - 2010
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BS, Chemistry, BiochemistryWayne State University, Department of Chemistry, Detroit, Michigan, 48202, United States
1999 - 2007
Center Memberships
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Center MemberAI and Digital Health Innovation
Research Overview
A tumor tissue biopsy is unfeasible for monitoring tumor evolution and represents one local area of a single lesion. Liquid biopsies like circulating, cell-free tumor DNA (ctDNA), have revolutionized non-invasive disease monitoring representing the entire disease, and can detect some targetable emerging driver mutations. Inclusion of single-cell analysis of circulating tumor cells (CTC), which are whole, intact cancer cells isolated from blood, promises to provide more complex, multi-omic information that may reveal the evolving landscape of a patient's cancer in real time. Dr. Cani has perfected single-CTC genomic profiling for the detection of targetable precision and immuno-oncology alterations, and has made considerable progress into single-CTC transcriptomic profiling. Together with the analysis of additional single-CTC omics approaches, in combination with tissue and ctDNA, and synergizing with the rich pipeline of molecularly informed therapies in the near future, his goal is to develop a platform that monitors the tumor molecular evolution for emerging resistance mechanisms and treatment strategies. This strategy can be tested in prospective interventional precision/immuno-oncology trials in patients with CTC-rich metastatic tumors like those of the breast, prostate, and others.
Recent Publications
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Wilson D, Dolce E, Cobain E, Thomas D, Rae J, Hayes D, Cani A. 2026 May 8;Proceeding / Abstract / PosterSingle Cell RNA Sequencing of Circulating Tumor Cells from Metastatic Breast Cancer Patients Reveals Heterogenous Expression of Cancer Driving Genes
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Wilson D, Dolce E, Cobain E, Thomas D, Rae J, Hayes D, Cani A. 2026 Mar 6;Proceeding / Abstract / PosterSingle Cell RNA Sequencing of Circulating Tumor Cells from Metastatic Breast Cancer Patients Reveals Heterogenous Expression of Cancer Driving Genes
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Wilson D, Dolce E, Cobain E, Thomas D, Rae J, Hayes D, Cani A. 2026 Mar 7;Proceeding / Abstract / PosterSingle-Cell RNA Sequencing of Circulating Tumor Cells from Metastatic Breast Cancer Patients Reveals Heterogenous Expression of Cancer Driving Genes
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Cani AK, Dolce EM, Darga EP, Hu K, Liu C, Robinson D, Wu Y, Paoletti C, Luker GD, Tomlins SA, Udager AM, Henderson NC, Thomas DG, Rae JM, Arul CM, Cobain EF, Hayes DF. Clinical Cancer Research, 2026 Feb 23; 32 (4_Supplement): ps2-07-22-ps2-07-22Journal ArticleAbstract PS2-07-22: Serial, multi-omic, multi-analyte, liquid biopsy monitoring of metastatic lobular breast cancer to detect clinically-relevant heterogeneity and evolution
DOI:10.1158/1557-3265.sabcs25-ps2-07-22 -
Cani A, Dolce E, Darga E, Hu K, Liu C-J, Robinson D, Wu Y-M, Paoletti C, Luker G, Tomlins S, Udager A, Henderson N, Thomas D, Rae J, Chinnaiyan A, Cobain E, Hayes D. Clinical Cancer Research, 2025 Dec 9; 32 (4_Supplement):Proceeding / Abstract / PosterAbstract PS2-07-22: Serial, multi-omic, multi-analyte, liquid biopsy monitoring of metastatic lobular breast cancer to detect clinically-relevant heterogeneity and evolution.
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Cani A, Dolce E, Darga E, Hu K, Liu C-J, Robinson D, Wu Y-M, Paoletti C, Luker G, Tomlins S, Udager A, Henderson N, Thomas D, Rae J, Chinnaiyan A, Cobain E, Hayes D. 2025 Sep 24;Proceeding / Abstract / PosterSerial, multi-omic, multi-analyte, liquid biopsy monitoring of metastatic lobular breast cancer to detect clinically-relevant heterogeneity and evolution
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Hernandez-Nunez I, Urman A, Zhang X, Jacob W, Li Q, Mao F, Cani A, Chen S, Dawlaty M, Rao RC, Ruzycki P, Edwards J, Clark B. 2025 May 4;Proceeding / Abstract / PosterActive DNA demethylation is required for photoreceptors fate specification and function
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Hernández-Núñez I, Urman A, Zhang X, Jacobs W, Hoffman C, Rebba S, Harding EG, Li Q, Mao F, Cani AK, Chen S, Dawlaty MM, Rao RC, Ruzycki PA, Edwards JR, Clark BS. 2025 Feb 3;PreprintActive DNA demethylation is upstream of rod-photoreceptor fate determination and required for retinal development.
DOI:10.1101/2025.02.03.636318 PMID: 39975078