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Bonnie Liu
Researcher at Genentech
Publications - 14
Citations - 2239
Bonnie Liu is an academic researcher from Genentech. The author has contributed to research in topics: MAPK/ERK pathway & Kinase. The author has an hindex of 9, co-authored 13 publications receiving 1957 citations.
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Journal ArticleDOI
RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth
Georgia Hatzivassiliou,Kyung Song,Ivana Yen,Barbara J. Brandhuber,Daniel Anderson,Ryan Alvarado,Mary J. C. Ludlam,David Stokoe,Susan L. Gloor,Guy Vigers,Tony Morales,Ignacio Aliagas,Bonnie Liu,Steve Sideris,Klaus P. Hoeflich,Bijay S. Jaiswal,Somasekar Seshagiri,Hartmut Koeppen,Marcia Belvin,Lori Friedman,Shiva Malek +20 more
TL;DR: It is demonstrated that ATP-competitive kinase inhibitors can have opposing functions as inhibitors or activators of signalling pathways, depending on the cellular context, which provides new insights into the therapeutic use of ATP- competitive RAF inhibitors.
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Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors
Anneleen Daemen,David A. Peterson,Nisebita Sahu,Ron McCord,Xiangnan Du,Bonnie Liu,Katarzyna Kowanetz,Rebecca Hong,John Moffat,Min Gao,Aaron Boudreau,Rana Mroue,Laura Corson,Thomas O'Brien,Jing Qing,Deepak Sampath,Mark Merchant,Robert L. Yauch,Gerard Manning,Jeffrey Settleman,Georgia Hatzivassiliou,Marie Evangelista +21 more
TL;DR: This paper identified three highly distinct metabolic subtypes in pancreatic ductal adenocarcinoma (PDAC) using broad metabolite profiling, which corresponded to differences in cell sensitivity to inhibitors of glycolysis, glutamine metabolism, lipid synthesis, and redox balance.
Journal ArticleDOI
ERK Inhibition Overcomes Acquired Resistance to MEK Inhibitors
Georgia Hatzivassiliou,Bonnie Liu,Carol O'Brien,Jill M. Spoerke,Klaus P. Hoeflich,Peter M. Haverty,Robert Soriano,William F. Forrest,Sherry Heldens,Huifen Chen,Karen Toy,Connie Ha,Wei Zhou,Kyung Song,Lori Friedman,Lukas C. Amler,Garret M. Hampton,John Moffat,Marcia Belvin,Mark R. Lackner +19 more
TL;DR: The data suggest that tumors with acquired MEK inhibitor resistance remain dependent on the MAPK pathway and are therefore sensitive to inhibitors that act downstream of the mutated MEK target, and provide a rationale for cotargeting multiple nodes within theMAPK signaling cascade in K-ras mutant tumors to maximize therapeutic benefit for patients.
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A transcriptional MAPK Pathway Activity Score (MPAS) is a clinically relevant biomarker in multiple cancer types.
Marie-Claire Wagle,Daniel C. Kirouac,Christiaan Klijn,Bonnie Liu,Shilpi Mahajan,Melissa R. Junttila,John Moffat,Mark Merchant,Ling Huw,Matthew Wongchenko,Kwame Okrah,Shrividhya Srinivasan,Zineb Mounir,Teiko Sumiyoshi,Peter M. Haverty,Robert L. Yauch,Yibing Yan,Omar Kabbarah,Garret Hampton,Lukas C. Amler,Saroja Ramanujan,Mark R. Lackner,Shih-Min A. Huang,Shih-Min A. Huang +23 more
TL;DR: An index that aggregates expression levels of 10 genes involved in modulating the mitogen-activated protein kinase (MAPK) pathway performed as well or better than other more complicated, genome-based tools at predicting whether drugs that inhibit MAPK-related enzymes were active against tumor cell lines.
Journal ArticleDOI
Pyrazolopyridine Inhibitors of B-Raf(V600E). Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors.
Steve Wenglowsky,Li Ren,Kateri A. Ahrendt,Ellen R. Laird,Ignacio Aliagas,Bruno Alicke,Alexandre J. Buckmelter,Edna F. Choo,Victoria Dinkel,Bainian Feng,Susan L. Gloor,Stephen E. Gould,Stefan Gross,Janet Gunzner-Toste,Joshua D. Hansen,Georgia Hatzivassiliou,Bonnie Liu,Kim Malesky,Simon Mathieu,Brad Newhouse,Nicholas J. Raddatz,Yingqing Ran,Sumeet Rana,Nikole Randolph,Tyler Risom,Joachim Rudolph,Scott Savage,LeAnn T. Selby,Michael Shrag,Kyung Song,Hillary L. Sturgis,Walter C. Voegtli,Zhaoyang Wen,Brandon S. Willis,Richard Woessner,Wen-I Wu,Wendy B. Young,Jonas Grina +37 more
TL;DR: Optimization led to the identification of 3-methoxy pyrazolopyridines 17 and 19, potent, selective, and orally bioavailable agents that inhibited tumor growth in a mouse xenograft model driven by B-Raf(V600E) with no effect on body weight.