基本信息
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Career Trajectory
Bio
Our current work is focused on:
Defining the molecular basis of oxygen sensing in the pathways that regulate mTOR and UPR signaling during hypoxia. We are currently studying the contribution of oxygen to protein folding and maturation in the endoplasmic reticulum.
Determining changes in gene expression downstream of hypoxic signaling pathways. These studies utilize high-throughput genomic methods to characterize changes in transcription, translation and protein production. Our group believes that hypoxia regulated proteins will be useful for both diagnostic and therapeutic purposes.
Understanding how hypoxic response pathways influence the biology of tumor cells in ways that affect patient prognosis. The signaling pathways regulated by oxygen control multiple cellular processes that are important for tumor cell growth, response to stress, and survival. These include regulation of metastasis, DNA repair, autophagy, and metabolism.
Assessing the potential of targeting hypoxic responses for improved treatment of cancer. This work involves the creation of tumor models that allow genetic manipulation of various components of hypoxic response pathways in established tumors in mice. The importance of different hypoxic response pathways is evaluated by monitoring changes in tumor metabolism, the tumor microenvironment, tumor growth, and response to treatment.
Discovery of vulnerabilities in cancer that are manifested only within the unique microenvironment of tumors. Our group believes that cancer associated genetic alterations influence tumor hypoxia and metabolism in ways that can be exploited for therapy and we are using high-throughput genomic tools such as RNA interference screens to identify novel molecular targets.
Defining the molecular basis of oxygen sensing in the pathways that regulate mTOR and UPR signaling during hypoxia. We are currently studying the contribution of oxygen to protein folding and maturation in the endoplasmic reticulum.
Determining changes in gene expression downstream of hypoxic signaling pathways. These studies utilize high-throughput genomic methods to characterize changes in transcription, translation and protein production. Our group believes that hypoxia regulated proteins will be useful for both diagnostic and therapeutic purposes.
Understanding how hypoxic response pathways influence the biology of tumor cells in ways that affect patient prognosis. The signaling pathways regulated by oxygen control multiple cellular processes that are important for tumor cell growth, response to stress, and survival. These include regulation of metastasis, DNA repair, autophagy, and metabolism.
Assessing the potential of targeting hypoxic responses for improved treatment of cancer. This work involves the creation of tumor models that allow genetic manipulation of various components of hypoxic response pathways in established tumors in mice. The importance of different hypoxic response pathways is evaluated by monitoring changes in tumor metabolism, the tumor microenvironment, tumor growth, and response to treatment.
Discovery of vulnerabilities in cancer that are manifested only within the unique microenvironment of tumors. Our group believes that cancer associated genetic alterations influence tumor hypoxia and metabolism in ways that can be exploited for therapy and we are using high-throughput genomic tools such as RNA interference screens to identify novel molecular targets.
Research Interests
Papers共 33 篇Author StatisticsCo-AuthorSimilar Experts
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Sandy Che-Eun S Lee, Andrea Hye An Pyo, Helia Mohammadi, Ji Zhang,Anna Dvorkin-Gheva,Lucie Malbeteau,Stephen Chung,Shahbaz Khan,M Teresa Ciudad,Vincent Rondeau,Rob A Cairns, Thomas Kislinger,Tracy L McGaha,Bradly G Wouters, Julie A Reisz,Rachel Culp-Hill, Angelo D'Alessandro,Courtney L Jones,Marianne Koritzinsky
Hilda Mujčić,Anika Nagelkerke,Kasper M.A. Rouschop, Stephen S. Chung,Naz Chaudary, Paul N. Span,Blaise Clarke, Michael Milosevic,Jenna Sykes,Rićhard P. Hill,Marianne Koritzinsky,Bradly G. Wouters
openalex
Sharon L. Walmsley,Leah Szadkowski,Bradly Wouters,Rosemarie Clarke,Karen Colwill,Paula Rochon,Michael Brudno, Rizanni Ravindran,Janet Raboud,Allison McGeer,Amit Oza,Christopher Graham,Amanda Silva,Dorin Manase, Peter Maksymowsky,Laura Parente, Roaya Monica Dayam,Jacqueline Simpson,Adrian Pasculescu,Anne-Claude Gingras
Social Science Research Network (2022)
Kulandaimanuvel Antony Michealraj,Sachin A. Kumar,Leo J. Y. Kim,Florence M. G. Cavalli,David Przelicki,John B. Wojcik,Alberto Delaidelli,Andrea Bajic,Olivier Saulnier,Graham MacLeod,Ravi N. Vellanki,Maria C. Vladoiu,Paul Guilhamon,Winnie Ong,John J. Y. Lee,Yanqing Jiang,Borja L. Holgado, Alex Rasnitsyn,Ahmad A. Malik,Ricky Tsai,Cory M. Richman,Kyle Juraschka,Joonas Haapasalo,Evan Y. Wang,Pasqualino De Antonellis,Hiromichi Suzuki,Hamza Farooq,Polina Balin,Kaitlin Kharas,Randy Van Ommeren,Olga Sirbu,Avesta Rastan, Stacey L. Krumholtz,Michelle Ly,Moloud Ahmadi,Genevieve Deblois,Dilakshan Srikanthan,Betty Luu,James Loukides,Xiaochong Wu,Livia Garzia,Vijay Ramaswamy,Evgeny Kanshin,Maria Sanchez-Osuna,Ibrahim El-Hamamy,Fiona J. Coutinho,Panagiotis Prinos, Sheila Singh,Laura K. Donovan,Craig Daniels,Daniel Schramek, Mike Tyers,Samuel Weiss,Lincoln D. Stein,Mathieu Lupien,Bradly G. Wouters,Benjamin A. Garcia,Cheryl H. Arrowsmith,Poul H. Sorensen,Stephane Angers,Nada Jabado,Peter B. Dirks,Stephen C. Mack,Sameer Agnihotri,Jeremy N. Rich,Michael D. Taylor
Neuro-oncology advancesno. Supplement_1 (2021): i15-i16
Pedro H. Boasquevisque, Verena Schoeneberger, Laura Caporiccio,Ravi Vellanki,Marianne Koritzinsky,Bradly G. Wouters
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Author Statistics
#Papers: 33
#Citation: 687
H-Index: 14
G-Index: 22
Sociability: 5
Diversity: 2
Activity: 30
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