Jennifer Pietenpol | |
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Born | July 18, 1964 |
Education | BS, Biology, 1986, Carleton College PhD, 1990, Vanderbilt University Postdoc, Johns Hopkins University |
Known for | p53, p73, Breast Cancer, Triple Negative Breast Cancer, VICC |
Scientific career | |
Institutions | Johns Hopkins University Vanderbilt University |
Jennifer Pietenpol (born 1964) is Chief Scientific and Strategic Officer, Executive Vice-President for Research, and the Ingram Professor of Cancer Research at Vanderbilt University Medical Center. [1] Pietenpol additionally serves as the Chief Scientific Advisor to the Susan G. Komen Foundation for breast cancer. [2]
Pietenpol's early research focused on the signaling of the p53 gene within the breast cancer family, specifically Triple Negative Breast Cancer. [3] [4] [5] Pietenpol used a combined approach of bioinformatics and genetics to make discoveries on the signaling behavior of the p53 gene family. [6] [7]
Pietenpol serves as an elected fellow of the American Association for the Advancement of Science (2012) and the American Association for Cancer Research Academy (2022). [3] In 2008 she was appointed by President George Bush to serve on the National Cancer Advisory Board for the National Cancer Institute. [8] In 2016 she was selected to serve on then Vice-President Joe Biden's National Cancer Moonshot Program's Blue Ribbon Panel. [9] [10]
Pietenpol studied biology at Carleton College in Northfield, Minnesota, where she now serves on the board of trustees. [11] She was a student athlete and still holds some of Carleton's volleyball and track and field team records. [12] [13] She received her PhD in cell biology at Vanderbilt University School of Medicine in 1990. [14] She later did postgraduate studies at Johns Hopkins School of Medicine. She was an assistant professor of Biochemistry at Vanderbilt from 1994. [15]
Pietenpol and her research group have developed techniques for analysis of p53 and p53 family member chromatin binding and identification of p53 family target genes. [16] [17] [18] Her team is also responsible for delineating p73 binding sites within the mammal the genome and the discovery that p73, another mammal protein gene, is required for ovarian folliculogenesis, multiciliogenesis, and certain regulation of the Foxj1-associated genes within mammals. [19] [20]
Her team successfully classified TNBC into 4 molecular subtypes―basal-like 1 (BL1), basal-like 2 (BL2), mesenchymal (M), and luminal androgen receptor (LAR). This was performed by the integration of molecular genomic techniques with bioinformatics, a tenant of Pietenpol's work. [21] [22] [23]
Recently, she and her team has focused on better understanding LAR TNBC, which is a rare subtype of TNBC that expresses androgen receptors, making it difficult to clinically treat. [24] [25]
Pietenpol has published over 250 scientific papers, which have been cited nearly 20,000 times, in journals including Nature , Cell , Cancer Research , and The Journal of Clinical Investigation . [26] [27]
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