J
James N. Ingle
Researcher at Mayo Clinic
Publications - 403
Citations - 52917
James N. Ingle is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Breast cancer & Tamoxifen. The author has an hindex of 82, co-authored 387 publications receiving 47883 citations. Previous affiliations of James N. Ingle include McMaster University & University of Rochester.
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Journal ArticleDOI
Body Mass Index, PAM50 Subtype, and Outcomes in Node-Positive Breast Cancer: CALGB 9741 (Alliance)
Jennifer A. Ligibel,Constance Cirrincione,Minetta C. Liu,Marc L. Citron,James N. Ingle,William J. Gradishar,Silvana Martino,William Sikov,Richard Alan Michaelson,Elaine R. Mardis,Charles M. Perou,Matthew J. Ellis,Eric P. Winer,Clifford A. Hudis,Donald A. Berry,William T. Barry +15 more
TL;DR: BMI at diagnosis was a statistically significant prognostic factor in a group of patients receiving optimally dosed chemotherapy, and additional research is needed to determine the impact of weight loss on breast cancer outcomes.
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Establishing and characterizing patient-derived xenografts using pre-chemotherapy percutaneous biopsy and post-chemotherapy surgical samples from a prospective neoadjuvant breast cancer study.
Jia Yu,Bo Qin,Ann M. Moyer,Jason P. Sinnwell,Kevin J. Thompson,John A. Copland,Laura A. Marlow,James L. Miller,Ping Yin,Bowen Gao,Katherine Minter-Dykhouse,Xiaojia Tang,Sarah A. McLaughlin,Alvaro Moreno-Aspitia,Anthony C. Schweitzer,Yan Lu,Jason Hubbard,Donald W. Northfelt,Richard Gray,Katie N. Hunt,Amy Lynn Conners,Vera J. Suman,Krishna R. Kalari,James N. Ingle,Zhenkun Lou,Daniel W. Visscher,Richard M. Weinshilboum,Judy C. Boughey,Matthew P. Goetz,Liewei Wang +29 more
TL;DR: The generation of PDX models both sensitive and resistant to standard NAC is feasible and these models exhibit similar biological and drug response characteristics as the patients’ primary tumors, which may be useful for biomarker discovery and future drug development.
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Quality of life in MAP.3 (Mammary Prevention 3): A randomized, placebo-controlled trial evaluating exemestane for prevention of breast cancer
Elizabeth Maunsell,Paul E. Goss,Rowan T. Chlebowski,James N. Ingle,José E. Alés-Martínez,Gloria E. Sarto,Carol J. Fabian,Pascal Pujol,Amparao Ruiz,Andrew Cooke,Susan L. Hendrix,Debra W. Thayer,Kendrith M. Rowland,Pierre Dubé,Silvana Spadafora,Sandhya Pruthi,Lavina Lickley,Susan Ellard,Angela M. Cheung,Jean Wactawski-Wende,Karen A. Gelmon,D. Johnston,Andrea Hiltz,Michael Brundage,Joseph L. Pater,Dongsheng Tu,Harriet Richardson +26 more
TL;DR: Exemestane given for prevention has limited negative impact on menopause-specific and health-related QOL in healthy postmenopausal women at risk for breast cancer.
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Cooperative groups and community hospitals. Measurement of impact in the community hospitals
Colin B. Begg,Marvin Zelen,Paul P. Carbone,Eleanor T. McFadden,Harvey S. Brodovsky,Paul F. Engstrom,Alan K. Hatfield,James N. Ingle,Burton Schwartz,Leo L. Stolbach +9 more
TL;DR: Assessment of a community cancer control program in Eastern Cooperative Oncology Group demonstrated that 16% of patients surveyed in the affiliated community hospitals were being treated on a research protocol, with a clear relationship between disease stage and age in breast cancer patients.
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Inhibition of Cdk2 kinase activity selectively targets the CD44+/CD24−/Low stem-like subpopulation and restores chemosensitivity of SUM149PT triple-negative breast cancer cells
Mateusz Opyrchal,Jeffrey L. Salisbury,Ianko D. Iankov,Matthew P. Goetz,James A. McCubrey,Mario W. Gambino,Lorenzo Malatino,Giuseppe Puccia,James N. Ingle,Evanthia Galanis,Antonino B. D'Assoro +10 more
TL;DR: This study employs the luminal ER+ MCF-7 and the IBC SUM149PT breast cancer cell lines to establish the extent to which high grade of CIN and chemoresistance were mechanistically linked to the enrichment of CD44+/CD24low/− CSCs and proposes a novel therapeutic approach to restore chemosensitivity and delay recurrence of IBC tumors.