Sofia D Merajver
GreaterGood Breast Cancer Research Professor
Professor of Internal Medicine
Professor of Epidemiology
Internal Medicine
1500 East Medical Center Drive
Ann Arbor, MI 48109
[email protected]

Available to mentor

Sofia D Merajver
Professor
  • Center Memberships
  • Research Overview
  • Recent Publications
  • Center Memberships
    • Center Member
      Rogel Cancer Center
    • Center Member
      Center for Computational Medicine and Bioinformatics
    • Center Member
      Precision Health Initiative
    • Center Member
      Institute for Healthcare Policy and Innovation
    Research Overview

    Dr. Sofia D. Merajver is an expert in clinical and translational research and breast cancer genetics with multidisciplinary research interests in the molecular genetics of breast cancer, molecular translational research, novel therapeutics, environmental and lifestyle modifiers of risk, gene function, clinical cancer risk assessment, international breast cancer research and prevention, and global health of non-communicable disease, all of which are represented in her nearly 300 publications. Her laboratory studies aggressive forms of breast cancer, with inflammatory breast cancer being the primary model. Her research is both clinical and translational. Dr. Merajver laboratory has discovered genetic alterations that contribute to an especially malignant phenotype of breast cancer called inflammatory breast cancer (IBC). They have isolated and characterized two markers specific for inflammatory breast cancer: a novel transforming oncogene RhoC-GTPase and a tumor suppressor gene termed WISP3, which is a low affinity IGF-binding protein. The laboratory has embarked on the study of RhoC signaling in single live cells utilizing laser spectroscopic techniques and mathematical modeling. Dr. Merajver has designed, conducted, and supervised Phase I, II, and III interventional therapeutic trials and Phase III prevention trials. In recent years, Dr. Merajver has built a mathematical modeling research portfolio that focuses on theoretical and experimental approaches to understanding the integration between cellular signaling and metabolism in cancer, as well as the development of predictive biomarkers of drug response to conventional and targeted therapies. Dr. Merajver and colleagues are studying polymorphisms and mutations in new candidate tumor suppressor genes and their relationship to breast cancer risk in non-BRCA 1/2 families. Dr. Merajver has a portfolio of projects ranging from molecular genetics to epidemiology to clinical care that she organizes in international settings. In her tenure as Director of the university-wide center for Global Health, Dr. Merajver helped define the global health agenda for the University of Michigan and has created multi-lateral and multi-disciplinary platforms of research and education engagement in global health equity. Dr. Merajver is actively engaged in health disparities research ranging from molecular determinants of untoward outcomes in African Americans and economically disadvantaged minorities to low resource world populations in Africa and Latin America. She is especially well known as an educator and dedicated mentor of postdoctoral and pre-doctoral students and of junior faculty at the UM Medical School and the School of Public Health and at many institutions worldwide, where her former trainees are engaged in scientific work and leadership. Dr. Merajver has trained over 140 scientists in her career, 60 of whom are pre-doctoral or post-doctoral and 100% of them are engaged in cancer research at academic institutions, government, and industry. She has received numerous honors and awards and Dr. Merajver is the only faculty member in the University of Michigan Medical School who has received both the Dean’s Basic Science Research Award and the MICHR Distinguished Translational Mentor Award.

    Recent Publications See All Publications
    • Journal Article
      Upgrade Rates and Breast Cancer Development Among Germline Pathogenic Variant Carriers with High-Risk Breast Lesions.
      Laws A, Leonard S, Hershey E, Stokes S, Vincuilla J, Sharma E, Milliron K, Garber JE, Merajver SD, King TA, Pilewskie ML. Ann Surg Oncol, 2024 May; 31 (5): 3120 - 3127. DOI:10.1245/s10434-024-14947-0
      PMID: 38261128
    • Journal Article
      A Lipopeptidomimetic of Transcriptional Activation Domains Selectively Disrupts Med25 Protein‐Protein Interactions
      Pattelli ON, Valdivia EM, Beyersdorf MS, Regan CS, Rivas M, Hebert KA, Merajver SD, Cierpicki T, Mapp AK. Angewandte Chemie, DOI:10.1002/ange.202400781
    • Proceeding / Abstract / Poster
      Abstract 223: Precision medicine-based platform to guide the treatment of EML4-ALK fusion lung cancers and other NSCLC
      Merrill NM, Udager A, Qin A, Lagisetty K, Bao L, Cheng X, Madhi H, Banerjee A, Jahromi MS, Goo L, Kathawate V, Vandenburg B, Aikins M, Slayton M, Ulintz P, Qin Z, Liu C-J, Serhan H, Jefferies J, Ali MS, Navani V, Monument M, Kratz J, Smith A, Chang A, Kalemkerian G, Nagrath S, Hsu P, Soellner MB, Merajver SD. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 223 - 223. DOI:10.1158/1538-7445.am2024-223
    • Journal Article
      Abstract 351: Quaratusugene ozeplasmid mediated TUSC2 upregulation in EML4-ALK bearing non-small cell lung carcinoma can induce cellular apoptosis
      Banerjee A, Busette N, Berger MS, Soellner MB, Qin A, Merajver SD, Merrill NM. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 351 - 351. DOI:10.1158/1538-7445.am2024-351
    • Journal Article
      Abstract 431: Malic enzyme 2 inhibition reveals metabolic vulnerability in serine-dependent triple-negative breast cancer
      Slayton MD, Farah ZA, Jeon JH, Achreja A, Krinkel B, Nilaj B, Eu Y-H, Sung J, Rosenfeld A, Lui A, Collard M, Bao L, Cheng X, Kleer C, Loomes K, Nagrath D, Merajver SD. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 431 - 431. DOI:10.1158/1538-7445.am2024-431
    • Journal Article
      Abstract 4548: Discovering novel ALK-lung carcinoma therapeutic strategies by identifying combinations with Alectinib from ALK-positive lung carcinoma cell lines
      Madhi H, Serhan H, Vandecan NM, Qin Z, Liu A, Udager A, Merajver SD, Soellner MB, Merrill N. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 4548 - 4548. DOI:10.1158/1538-7445.am2024-4548
    • Journal Article
      Abstract 7091: Significance of the tryptophan catabolism pathway in triple-negative breast cancer shows potential targets in certain subsets relating to the serine pathway
      Jeon JH, Achreja A, Slayton M, Animasahun O, Nenwani M, Paserba M, Farah Z, Merajver SD, Nagrath D. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 7091 - 7091. DOI:10.1158/1538-7445.am2024-7091
    • Journal Article
      Abstract 7504: Longitudinal multi-omics characterization of circulating tumor cells from ALK positive NSCLC patients
      Chen Y, Fouladdel S, Ball H, Qin Z, Liu A, Cheng X, Bao L, Serhan H, Vandenburg B, Kathawate V, Goo L, Ulintz P, Merrill N, Udager A, Qin A, Merajver SD, Nagrath S. Cancer Research, 2024 Mar 22; 84 (6_Supplement): 7504 - 7504. DOI:10.1158/1538-7445.am2024-7504