J
John Repass
Researcher at University of Texas MD Anderson Cancer Center
Publications - 5
Citations - 537
John Repass is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Cancer & Transgene. The author has an hindex of 4, co-authored 5 publications receiving 495 citations.
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Journal ArticleDOI
NANOG promotes cancer stem cell characteristics and prostate cancer resistance to androgen deprivation
Collene R. Jeter,Bigang Liu,Xin Liu,Xin Liu,Xin-Xin Chen,Can Liu,Tammy Calhoun-Davis,John Repass,Holm Zaehres,Jianjun Shen,Dean G. Tang +10 more
TL;DR: Gain-of-function studies establish the integral role for NANOG in neoplastic processes and shed light on its mechanisms of action in tumorigenesis, as well as establishing the importance of CXCR4, IGFBP5, CD133 and ALDH1 in this work.
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IL7-hCD25 and IL7-Cre BAC transgenic mouse lines: new tools for analysis of IL-7 expressing cells.
John Repass,Micheline N. Laurent,Carla Carter,Boris Reizis,Mark T. Bedford,Kim Cardenas,Priyanka Narang,Mark Coles,Ellen R. Richie +8 more
TL;DR: Two bacterial artificial chromosome transgenic mouse lines are generated in which IL‐7 regulatory elements drive expression of either Cre recombinase or a human CD25 (hCD25) cell surface reporter molecule and these transgenic lines provide novel genetic tools to identifyIL‐7 producing cells in various tissues and to manipulate gene expression selectively in IL‐ 7 expressing cells.
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Dietary energy balance modulates prostate cancer progression in Hi-Myc mice.
Jorge Blando,Tricia Moore,Stephen D. Hursting,Guiyu Jiang,Achinto Saha,Linda M Beltran,Jianjun Shen,John Repass,Sara S. Strom,John DiGiovanni +9 more
TL;DR: Findings suggest that enhanced growth factor (Akt/mTORC1 and STAT3) and inflammatory (NFκB and cytokines) signaling may play a role in dietary energy balance effects on prostate cancer progression in Hi-Myc mice.
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Proteomic and pathway analyses reveal a network of inflammatory genes associated with differences in skin tumor promotion susceptibility in DBA/2 and C57BL/6 mice.
Jianjun Shen,Erika L. Abel,Penny K. Riggs,John Repass,Sean C. Hensley,Lisa J. Schroeder,Angelina Temple,Alexander Chau,S. Alex McClellan,Okkyung Rho,Kaoru Kiguchi,Michael D. Ward,O. John Semmes,Maria D. Person,Joe M. Angel,John DiGiovanni +15 more
TL;DR: It is suggested that differential expression of genes involved in inflammatory pathways in epidermis may play a key role in genetic differences in susceptibility to skin tumor promotion in DBA/2 and C57BL/6 mice.
Journal ArticleDOI
ATF3-Induced Mammary Tumors Exhibit Molecular Features of Human Basal-Like Breast Cancer.
Leqin Yan,Sally Gaddis,Luis Della Coletta,John Repass,Katherine Leslie Powell,Melissa S. Simper,Yueping Chen,Michelle Byrom,Yi Zhong,Kevin Lin,Bin Liu,Yue Lu,Jianjun Shen,Michael C. MacLeod +13 more
TL;DR: In this paper, the authors used RNA-Seq and microRNA (miRNA) microarrays to better define the molecular features of BK5.ATF3-derived mammary tumors.