Chefmikesf/sandbox/Scott W. Lowe | |
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Born | 1963 |
Nationality | American |
Citizenship | American |
Alma mater | |
Known for | p53 |
Scientific career | |
Fields | Cancer Genetics |
Institutions |
Scott William Lowe (born October 4, 1963) is Chair of the Cancer Biology and Genetics Program in the Sloan Kettering Institute at Memorial Sloan Kettering Cancer Center. He is recognized for his research on the tumor suppressor gene p53, which is mutated in nearly half of cancers.
Lowe was born in 1963 in Racine, Wisconsin. He enrolled at the University of Wisconsin-Madison in chemical engineering in 1982 before changing his major to biology. He worked for two years after graduation as a lab technician in a hypercholesterolemia lab. [1] Low entered the Massachusetts Institute of Technology (MIT) with an interest in oncogene cooperation in carcinogenesis, [2] and went on to earn his PhD studying the role of p53 in cancer development. [3] He stayed at MIT as a postdoctoral fellow with David Housman and Tyler Jacks. [3]
While at MIT, he showed that the tumor suppressor p53 is required for the cell death program that occurs in response to cytotoxic agents such as ionizing radiation and DNA-damaging chemotherapies. He moved from MIT to Cold Spring Harbor Laboratory, starting his own laboratory as a Cold Spring Harbor Laboratory Fellow in 1995 and continuing his work on p53. A key outcome of this research was the discovery of a process known as oncogene-induced senescence, which is now a well-established tumor suppressive program. [2] His laboratory's findings related to p53 gene mutation status and responsiveness of a tumor to chemotherapy was among the pieces of evidence that ushered in the era of personalized cancer medicine. [2] He eventually became Deputy Director of the CSHL Cancer Center. Much of his work has focused on the biological action of tumor suppressor genes, and the consequences of their mutation. [4] In collaboration with Gregory Hannon and Stephen Elledge, he has made extensive use of RNA interference to study the roles of tumor suppressor genes. He is also known for using genome-editing tools such as CRISPR to create valuable mouse models of different cancers. He moved to Memorial Sloan Kettering in 2011 to lead the Cancer Biology and Genetics Program in the Sloan Kettering Institute, where he has recently discovered mechanisms whereby senescence inducing therapies promote cancer cell immune surveillance (Ruscetti nature/cell). In 2015, Lowe continued his use of RNAi to study the tumor suppressor APC in colorectal cancer. He has been an HHMI Investigator since 2005. [5] In 2017, Dr. Lowe was elected to the United States National Academy of Sciences. [2] In 2019, Dr. Lowe was elected to the National Academy of Medicine. [6]
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Chefmikesf/sandbox/Scott W. Lowe | |
---|---|
![]() | |
Born | 1963 |
Nationality | American |
Citizenship | American |
Alma mater | |
Known for | p53 |
Scientific career | |
Fields | Cancer Genetics |
Institutions |
Scott William Lowe (born October 4, 1963) is Chair of the Cancer Biology and Genetics Program in the Sloan Kettering Institute at Memorial Sloan Kettering Cancer Center. He is recognized for his research on the tumor suppressor gene p53, which is mutated in nearly half of cancers.
Lowe was born in 1963 in Racine, Wisconsin. He enrolled at the University of Wisconsin-Madison in chemical engineering in 1982 before changing his major to biology. He worked for two years after graduation as a lab technician in a hypercholesterolemia lab. [1] Low entered the Massachusetts Institute of Technology (MIT) with an interest in oncogene cooperation in carcinogenesis, [2] and went on to earn his PhD studying the role of p53 in cancer development. [3] He stayed at MIT as a postdoctoral fellow with David Housman and Tyler Jacks. [3]
While at MIT, he showed that the tumor suppressor p53 is required for the cell death program that occurs in response to cytotoxic agents such as ionizing radiation and DNA-damaging chemotherapies. He moved from MIT to Cold Spring Harbor Laboratory, starting his own laboratory as a Cold Spring Harbor Laboratory Fellow in 1995 and continuing his work on p53. A key outcome of this research was the discovery of a process known as oncogene-induced senescence, which is now a well-established tumor suppressive program. [2] His laboratory's findings related to p53 gene mutation status and responsiveness of a tumor to chemotherapy was among the pieces of evidence that ushered in the era of personalized cancer medicine. [2] He eventually became Deputy Director of the CSHL Cancer Center. Much of his work has focused on the biological action of tumor suppressor genes, and the consequences of their mutation. [4] In collaboration with Gregory Hannon and Stephen Elledge, he has made extensive use of RNA interference to study the roles of tumor suppressor genes. He is also known for using genome-editing tools such as CRISPR to create valuable mouse models of different cancers. He moved to Memorial Sloan Kettering in 2011 to lead the Cancer Biology and Genetics Program in the Sloan Kettering Institute, where he has recently discovered mechanisms whereby senescence inducing therapies promote cancer cell immune surveillance (Ruscetti nature/cell). In 2015, Lowe continued his use of RNAi to study the tumor suppressor APC in colorectal cancer. He has been an HHMI Investigator since 2005. [5] In 2017, Dr. Lowe was elected to the United States National Academy of Sciences. [2] In 2019, Dr. Lowe was elected to the National Academy of Medicine. [6]
{{
cite web}}
: CS1 maint: url-status (
link)