Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Lynda Bennett"'
Autor:
Stephen X. Skapek, Yanbin Zheng, Priscilla Liem, Qinbo Zhou, Jing Liu, Jared C. Hooks, Lynda Bennett, Lin Xu, Yen-Ting Liu
Disruption of the CDKN2A (INK4A/ARF) and B (INK4B) genes, which encode three function-independent tumor suppressors, is one of the most common events in human cancer. Because their relative importance in tumor prevention appears to be species- and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdacb882248483cb660a5ce1f2ea3454
https://doi.org/10.1158/1541-7786.c.6540370
https://doi.org/10.1158/1541-7786.c.6540370
Autor:
Stephen X. Skapek, Yanbin Zheng, Priscilla Liem, Qinbo Zhou, Jing Liu, Jared C. Hooks, Lynda Bennett, Lin Xu, Yen-Ting Liu
Supplementary Table S1. Sequences of siRNAs, sgRNAs and primers for regular PCR, qRT-PCR and ChIP-qPCR Figure S1. Global analysis of ARF regulation from The Cancer Genome Atlas (TCGA). Figure S2. The status of DNA methylation at promoter regions of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15abb094d51e6a185b5fbcd3ea41b526
https://doi.org/10.1158/1541-7786.22512907.v1
https://doi.org/10.1158/1541-7786.22512907.v1
Publikováno v:
Cancer Research. 83:654-654
Elevated levels of immunosuppressive myeloid-derived suppressor cells (MDSCs) circulate in the peripheral blood or infiltrate the tumors as well as ascites in ovarian cancer patients, however the cause for this observed phenotype is unknown. MDSCs co
Publikováno v:
Cancer Research. 83:3697-3697
Introduction: Cancer cells often develop a program of metabolic adaptability and epigenetic remodelling to promote gene expression changes causing cancerous cell proliferation and invasion. The metabolic-epigenetic axis as a an underlying mechanism o
Autor:
Jared C. Hooks, Yanbin Zheng, Yen Ting Liu, Jing Liu, Lin Xu, Priscilla Liem, Stephen X. Skapek, Lynda Bennett, Qinbo Zhou
Publikováno v:
Molecular Cancer Research. 17:1854-1866
Disruption of the CDKN2A (INK4A/ARF) and B (INK4B) genes, which encode three function-independent tumor suppressors, is one of the most common events in human cancer. Because their relative importance in tumor prevention appears to be species- and co
Autor:
Candace Frerich, Ishrat Durdana, Ariella Hanker, Carlos L. Arteaga, Lynda Bennett, Suzanne Conzen
Publikováno v:
Cancer Research. 82:2699-2699
While considered uncommon, there are an estimated 39,000 new invasive lobular carcinoma (ILC) cases in the US yearly, making it the sixth most common among all tumor types. ILC is recognized for unique metastatic organotropism. Its propensity to meta
Publikováno v:
Cancer Research. 82:1335-1335
Immunosuppressive cells abundantly infiltrate tumors during cancer progression. Notably, immunosuppressive myeloid-derived suppressor cells (MDSCs) have recently been identified as a heterogeneous cell population that expand during tumor-associated i
Autor:
Tobias Wijshake, Beth Levine, John G. Doench, Yang Xie, Guanghua Xiao, Beibei Chen, Lynda Bennett, Lin Zhong, Zhongju Zou
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Beclin 1, an essential autophagy protein, is important for tumor suppression in mice, as well as in human breast and ovarian cancers. However, it is not well understood how Beclin 1 acts as a tumor suppressor. By performing a genetic scr
Publikováno v:
The Journal of Immunology. 208:178.10-178.10
Myeloid-derived suppressor cells (MDSCs) have been identified as a heterogeneous cell population that expand during tumor progression and infiltrate the tumor, peripheral blood, as well as ascites of ovarian cancer patients. MDSCs contribute to tumor
Autor:
Sangita C. Sinha, Beth Levine, Zhongju Zou, Li Yu, Yue Li, Lynda Bennett, Y. Zhao, Daxiao Sun
Publikováno v:
Autophagy
article-version (VoR) Version of Record
article-version (VoR) Version of Record
A key mediator of macroautophagy/autophagy induction is the class III phosphatidylinositol 3-kinase complex I (PtdIns3K-C1) consisting of PIK3C3/VPS34, PIK3R4/VPS15, BECN1, and ATG14. Although several proteins are known to enhance or decrease PtdIns3