C
Chunxiao Xu
Researcher at Harvard University
Publications - 47
Citations - 6293
Chunxiao Xu is an academic researcher from Harvard University. The author has contributed to research in topics: Lung cancer & Cancer. The author has an hindex of 29, co-authored 43 publications receiving 5446 citations. Previous affiliations of Chunxiao Xu include Drexel University & Merck Serono.
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Journal ArticleDOI
miR-122, a mammalian liver-specific microRNA, is processed from hcr mRNA and may downregulate the high affinity cationic amino acid transporter CAT-1.
Jinhong Chang,Emmanuelle Nicolas,Debora S. Marks,Chris Sander,Anthony Lerro,Marie Annick Buendia,Chunxiao Xu,William S. Mason,Thomas Moloshok,Roque Bort,Kenneth S. Zaret,John M. Taylor +11 more
TL;DR: These studies show that miR-122, a 22-nucleotide microRNA, is derived from a liver-specific non-coding polyadenylated RNA transcribed from the gene hcr, which may be a specific mRNA target, CAT-1, which is expressed in all mammaliantissues but with lower levels in adult liver.
Journal ArticleDOI
Overcoming EGFR(T790M) and EGFR(C797S) resistance with mutant-selective allosteric inhibitors
Yong Jia,Cai-Hong Yun,Eun Young Park,Dalia Ercan,Mari Manuia,Jose Juarez,Chunxiao Xu,Kevin Rhee,Ting Chen,Haikuo Zhang,Sangeetha Palakurthi,Jaebong Jang,Gerald Lelais,Michael DiDonato,Badry Bursulaya,Pierre-Yves Michellys,Robert Epple,Thomas H. Marsilje,Matthew McNeill,Wenshuo Lu,Jennifer L. Harris,Bender Steven Lee,Kwok-Kin Wong,Pasi A. Jänne,Michael J. Eck +24 more
TL;DR: Rational discovery of EAI045 is described, an allosteric inhibitor that targets selected drug-resistant EGFR mutants but spares the wild type receptor and shows dramatic synergy of cetuximab, an antibody therapeutic that blocks EGFR dimerization, rendering the kinase uniformly susceptible to theAllosteric agent.
Journal ArticleDOI
Mutations in the DDR2 Kinase Gene Identify a Novel Therapeutic Target in Squamous Cell Lung Cancer
Peter S. Hammerman,Martin L. Sos,Alex H. Ramos,Chunxiao Xu,Amit Dutt,Wenjun Zhou,Lear E. Brace,Brittany Woods,Wenchu Lin,Jianming Zhang,Xianming Deng,Sang Min Lim,Stefanie Heynck,Martin Peifer,Jeffrey R. Simard,Michael S. Lawrence,Robert C. Onofrio,Helga B. Salvesen,Danila Seidel,Thomas Zander,Johannes M. Heuckmann,Alex Soltermann,Holger Moch,Mirjam Koker,Frauke Leenders,Frauke Leenders,Franziska Gabler,Silvia Querings,Sascha Ansén,Elisabeth Brambilla,Christian Brambilla,Philippe Lorimier,Odd Terje Brustugun,Åslaug Helland,Iver Petersen,Joachim H. Clement,Harry J.M. Groen,Wim Timens,Hannie Sietsma,Erich Stoelben,Juergen Wolf,David G. Beer,Ming-Sound Tsao,Megan Hanna,Megan Hanna,Charlie Hatton,Charlie Hatton,Michael J. Eck,Pasi A. Jänne,Bruce E. Johnson,Wendy Winckler,Heidi Greulich,Heidi Greulich,Adam J. Bass,Jeonghee Cho,Daniel Rauh,Nathanael S. Gray,Kwok-Kin Wong,Eric B. Haura,Roman K. Thomas,Matthew Meyerson,Matthew Meyerson +61 more
TL;DR: Findings suggest that gain-of-function mutations in DDR2 are important oncogenic events and are amenable to therapy with dasatinib, and provide a rationale for designing clinical trials with the FDA-approved drug d asatinib in patients with lung SCCs.
Journal ArticleDOI
A murine lung cancer co-clinical trial identifies genetic modifiers of therapeutic response
Zhao Chen,Katherine A. Cheng,Zandra E. Walton,Yuchuan Wang,Hiromichi Ebi,Takeshi Shimamura,Yan Liu,Tanya Tupper,Jing Ouyang,Jie Li,Peng Gao,Michele S. Woo,Chunxiao Xu,Masahiko Yanagita,Abigail Altabef,Shumei Wang,Charles Lee,Yuji Nakada,Christopher G. Peña,Yanping Sun,Yoko Franchetti,Catherine Yao,Amy Saur,Michael D. Cameron,Mizuki Nishino,D. Neil Hayes,Matthew D. Wilkerson,Patrick J. Roberts,Carrie B. Lee,Nabeel Bardeesy,Mohit Butaney,Lucian R. Chirieac,Daniel B. Costa,David M. Jackman,Norman E. Sharpless,Diego H. Castrillon,George D. Demetri,Pasi A. Jänne,Pier Paolo Pandolfi,Lewis C. Cantley,Andrew L. Kung,Jeffrey A. Engelman,Kwok-Kin Wong +42 more
TL;DR: It is demonstrated that concomitant loss of either p53 or Lkb1, two clinically relevant tumour suppressors, markedly impaired the response of Kras-mutant cancers to docetaxel monotherapy, highlighting the rationale for synchronous co-clinical trials.
Journal ArticleDOI
Enhanced preclinical antitumor activity of M7824, a bifunctional fusion protein simultaneously targeting PD-L1 and TGF-β
Yan Lan,Dong Zhang,Chunxiao Xu,Kenneth W. Hance,Bo Marelli,Jin Qi,Huakui Yu,Guozhong Qin,Aroop Sircar,Vivian M. Hernández,Molly H. Jenkins,Rachel E. Fontana,Amit M. Deshpande,George Locke,Helen Sabzevari,Laszlo Radvanyi,Kin-Ming Lo +16 more
TL;DR: Preclinical data demonstrate that simultaneous blockade of the PD-L1 and TGF-β pathways by M7824 elicits potent and superior antitumor activity relative to monotherapies.