Roxana Moslehi
Roxana Moslehi is an Iranian-born genetic epidemiologist.
Most of her research is dedicated to the study of cancer and cancer precursors. Born in Iran and raised in Iran and Canada, she is currently an associate professor[1] in Epidemiology and Biostatistics at the University at Albany, State University of New York (SUNY), where she has been teaching multiple courses, including those she developed in genetic and molecular epidemiology. Through her research, she has contributed to understanding hereditary causes of diseases and the influence of gene-environment interactions on the risk of developing disease.
Education
Roxana received her B.Sc. with honors, M.Sc., and Ph.D. degrees from the University of British Columbia (UBC) in Vancouver, Canada, following her Ph.D. under the mentorship of Drs. J.M. Friedman and Steven Narod completed a postdoctoral fellowship at the National Institutes of Health (NIH), Division of Cancer Epidemiology and Genetics (DCEG), under the supervision of Mitchell Gail. While a postdoctoral fellow at the NIH, she received an adjunct assistant professor position at George Washington University (GWU), where she co-taught a course entitled "controversies in cancer epidemiology".[2]
Research
The overarching theme of Roxana Moslehi's research has been identifying and characterizing cancer susceptibility genes. Working with Drs. Steven Narod and J.M. Friedman, her study was among the first to estimate the penetrance of BRCA1 and BRCA2 mutations for breast, ovarian and other cancers in a study of Jewish women with ovarian cancer.[3] Roxana expanded her studies of breast and ovarian cancer to other populations, including those in the Middle East, some understudied at the time. For example, through collaboration with physicians in Iran, Moslehi conducted studies on hereditary breast and ovarian cancer families, which led to the discovery of a novel BRCA1 mutation in the Iranian population.[4][5]
Roxana has also made significant contributions to research on modifiers of BRCA-associated breast and ovarian cancer risk[6][7] as well as to the understanding of mechanistic and population genetic aspects of the BRCA genes, now the most studied hereditary cancer predisposing genes in the human genome. In one such study, she investigated the impact of mutations in the BRCA1 and BRCA2 genes on female fertility as a potential mechanism influencing positive selection for BRCA mutations.[8] More recently, Roxana led an integrative genomics study of common breast cancer, which identified two previously unreported low- to moderate-risk breast cancer susceptibility gene candidates.[9]
Roxana Moslehi's hypotheses extend beyond the BRCA and other breast cancer susceptibility genes to genetic and biological mechanisms involved in other cancers and disorders. Recently, she published a series of studies on the adverse effects of abnormalities in DNA repair and transcription genes on human reproduction and development. Based on her novel clinical observations in trichothiodystrophy (TTD) families, Roxana developed the hypothesis that defects in the nucleotide excision repair and transcription genes have adverse effects on human fetal and placental development.[10] Subsequently, she proposed impairment of TFIIH-mediated function in transcription in placenta as one mechanism leading to gestational complications such as preeclampsia and highlighted the relevance of the fetal genotype and the exact genetic abnormality to this mechanism.[11][12][13] In addition to breast and ovarian cancer, Roxana has been conducting genetic and epidemiologic investigations of other cancer and cancer precursors, such as Colorectal adenoma,[14] Lung cancer[15] and Non-Hodgkin lymphoma.[16]
More recently, Moslehi was awarded a research grant from the National Institute of Allergy and Infectious Diseases (NIAID), NIH to conduct a study to explore the link between myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS), autoimmune disorders, and cancer.[17] In July 2021, Roxana gave a talk at a Sci Foo event organized by Google, Nature, and O’Reilly Media on the link between COVID-19 and ME/CFS.[18]
Awards
Roxana Moslehi is a recipient of multiple awards and honors, including the Graduate Teaching Assistant Award for Excellence in Teaching (UBC), a Biovision Fellowship from Académie des Sciences (France), two Awards for Research Excellence from the NIH, and the Golden Apple Award for Excellence in Teaching from School of Public Health at SUNY Albany.[19] Roxana also earned an invitation-only spot in the annual Science Foo Camp, where researchers, writers, educators, artists, policy makers, and investors exchange 'blue sky' ideas.[20] In December 2021, Roxana Moslehi was named as one of the recipients of the NIH Director's Scientific/Medical Awards for her efforts as a member of the COVID-19 Contact Investigations Team.[21]
References
- "Roxana Moslehi, State University of New York (SUNY)".
- "Roxana Moslehi | University at Albany". www.albany.edu. Retrieved 2021-12-18.
- Moslehi, R.; Chu, W.; Karlan, B.; Fishman, D.; Risch, H.; Fields, A.; Smotkin, D.; Ben-David, Y.; Rosenblatt, J.; Russo, D.; Schwartz, P. (April 2000). "BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer". American Journal of Human Genetics. 66 (4): 1259–1272. doi:10.1086/302853. ISSN 0002-9297. PMC 1288193. PMID 10739756.
- Moslehi, Roxana; Karimi-Nejad, M. Hassan; Ghafari, Vahraz; Narod, Steven (15 March 2003). "Analysis of BRCA1 and BRCA2 mutations in an Iranian family with hereditary breast and ovarian cancer syndrome". American Journal of Medical Genetics. 117A (3): 304–305. doi:10.1002/ajmg.a.10031. PMID 12599199. S2CID 27731736.
- Moslehi, Roxana; Kariminejad, M. Hassan; Ghafari, Vahraz; Narod, Steven (2003-03-15). "Analysis of BRCA1 and BRCA2 mutations in an Iranian family with hereditary breast and ovarian cancer syndrome". American Journal of Medical Genetics. Part A. 117A (3): 304–305. doi:10.1002/ajmg.a.10031. ISSN 1552-4825. PMID 12599199. S2CID 27731736.
- Narod, Steven A.; Risch, Harvey; Moslehi, Roxana; Dørum, Anne; Neuhausen, Susan; Olsson, Hakan; Provencher, Diane; Radice, Paolo; Evans, Gareth; Bishop, Susan; Brunet, Jean-Sébastien; Ponder, Bruce A.J.; Klijn, Jan G.M. (13 August 1998). "Oral Contraceptives and the Risk of Hereditary Ovarian Cancer". New England Journal of Medicine. 339 (7): 424–428. doi:10.1056/NEJM199808133390702. PMID 9700175.
- Modugno, Francesmary; Moslehi, Roxana; Ness, Roberta B.; Nelson, Deborah Brooks; Belle, Steven; Kant, Jeffrey A.; Wheeler, James E.; Wonderlick, Aimee; Fishman, David; Karlan, Beth; Risch, Harvey; Cramer, Daniel W.; Dube, Marie-Pierre; Narod, Steven A. (1 June 2003). "Reproductive factors and ovarian cancer risk in Jewish BRCA1 and BRCA2 mutation carriers (United States)". Cancer Causes & Control. 14 (5): 439–446. doi:10.1023/A:1024932427503. PMID 12946038. S2CID 40261099.
- Moslehi, Roxana; Singh, Ranjana; Lessner, Lawrence; Friedman, Jan M. (2009). "Impact of mutations on female fertility and offspring sex ratio". American Journal of Human Biology. 22 (2): 201–5. doi:10.1002/ajhb.20978. PMC 3739697. PMID 19642207.
- Moslehi, Roxana; Tsao, Hui-Shien; Zeinomar, Nur; Stagnar, Cristy; Fitzpatrick, Sean; Dzutsev, Amiran (2020-12-04). "Integrative genomic analysis implicates ERCC6 and its interaction with ERCC8 in susceptibility to breast cancer". Scientific Reports. 10 (1): 21276. Bibcode:2020NatSR..1021276M. doi:10.1038/s41598-020-77037-7. ISSN 2045-2322. PMC 7718875. PMID 33277540.
- Moslehi, R; Signore, C; Tamura, D; Mills, JL; DiGiovanna, JJ; Tucker, MA; Troendle, J; Ueda, T; Boyle, J; Khan, SG; Oh, K-S; Goldstein, AM; Kraemer, KH (April 2010). "Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development". Clinical Genetics. 77 (4): 365–373. doi:10.1111/j.1399-0004.2009.01336.x. PMC 3463936. PMID 20002457.
- Moslehi, Roxana; Kumar, Anil; Mills, James L.; Ambroggio, Xavier; Signore, Caroline; Dzutsev, Amiran (June 2012). "Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta". European Journal of Human Genetics. 20 (6): 626–631. doi:10.1038/ejhg.2011.249. PMC 3355251. PMID 22234153.
- Moslehi, Roxana; Mills, James L.; Signore, Caroline; Kumar, Anil; Ambroggio, Xavier; Dzutsev, Amiran (30 August 2013). "Integrative transcriptome analysis reveals dysregulation of canonical cancer molecular pathways in placenta leading to preeclampsia". Scientific Reports. 3 (1): 2407. Bibcode:2013NatSR...3E2407M. doi:10.1038/srep02407. PMC 3757356. PMID 23989136.
- Moslehi, Roxana; Ambroggio, Xavier; Nagarajan, Vijayaraj; Kumar, Anil; Dzutsev, Amiran (15 May 2014). "Nucleotide excision repair/transcription gene defects in the fetus and impaired TFIIH-mediated function in transcription in placenta leading to preeclampsia". BMC Genomics. 15 (1): 373. doi:10.1186/1471-2164-15-373. PMC 4229886. PMID 24885447.
- Moslehi, Roxana; Chatterjee, Nilanjan; Church, Timothy R; Chen, Jinbo; Yeager, Meredith; Weissfeld, Joel; Hein, David W; Hayes, Richard B (September 2006). "Cigarette smoking, N-acetyltransferase genes and the risk of advanced colorectal adenoma". Pharmacogenomics. 7 (6): 819–829. doi:10.2217/14622416.7.6.819. PMID 16981843.
- Tan, Xiang-Lin; Moslehi, Roxana; Han, WeiGuo; Spivack, Simon D. (2009). "Haplotype-tagging single nucleotide polymorphisms in the GSTP1 gene promoter and susceptibility to lung cancer". Cancer Detection and Prevention. 32 (5–6): 403–415. doi:10.1016/j.cdp.2009.02.004. PMC 3730463. PMID 19282111.
- Moslehi, Roxana; Devesa, Susan S.; Schairer, Catherine; Fraumeni, Joseph F. (5 July 2006). "Rapidly Increasing Incidence of Ocular Non-Hodgkin Lymphoma". JNCI. 98 (13): 936–939. doi:10.1093/jnci/djj248. PMID 16818858.
- Moslehi, Roxana. "Chronic Fatigue Syndrome, Immune Dysregulation, and Non-Hodgkin's Lymphoma".
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(help) - The Link Between COVID-19 and the Mysterious Illness, ME/CFS - Roxana Moslehi, retrieved 2021-11-29
- "Roxana Moslehi Awards and Honours". www.albany.edu. Retrieved 2021-11-29.
- "In Rarified Intellectual Air - University at Albany-SUNY". www.albany.edu. Retrieved 2021-12-18.
- "2021 OD Awards | NIH Director's Awards". directorsawards.hr.nih.gov. Retrieved 2021-12-23.