Evolution of tumors, and evolution generally, occurs by variation and selection. Variation creates the ability to evolve (evolvability). Whereas conventional therapies kill cells or stop them from growing (are anti- proliferative), proposed novel interventions that would inhibit the ability to evolve promise new and fundamentally different ways to inhibit oncogenesis and thwart resistance. The Cancer Evolvability Program (CE) aims to understand the fundamental underlying molecular mechanisms that generate variation and so drive tumor evolution; to develop new molecular approaches and tools to advance cancer diagnosis and therapy; and to develop with other CCSG programs the conceptual and technical frameworks for translational cancer research. The CE Program encompasses two themes, which focus on the two basic routes that generate variation: (1) Intrinsic: Genome and Phenotypic Plasticity (mutation, genome rearrangement, recombination, epigenetic and stochastic protein and RNA variation); and (2) Extrinsic: Infectious Oncogenesis and Microbiome, in which introduction of foreign genes, proteins, RNAs, and other molecules and genetic programs by infectious agents (viruses, microbes, microbiome) promote (or prevent) oncogenesis. The CCSG supports this research program by providing key shared resources, particularly Cytometry and Cell Sorting, Integrated Microscopy, Genomic and RNA Profiling, and Proteomics; as well as administrative support for meetings, clubs and interest groups, and pilot funding and recruitment funds. The CE Program currently has 31 members from ten departments in two institutions. Thirty members have primary appointments at Baylor College of Medicine, one member has a primary appointment at the University of Texas and therefore is an adjunct member. The Cancer Evolvability Program currently has $9.6M in peer-reviewed funding (direct costs per annum), $2.6M from NCI and $1.5M in other peer reviewed funding mostly from the Cancer Prevention and Research Initiative of Texas (CPRIT). Most of this is in the form of R01 grants. Members of the Cancer Evolvability Program published a total of 452 cancer-related papers in the previous funding period: 28% were inter-programmatic, 13% were intra-programmatic, and 50% were ?inter-institutional? (collaborations outside the Dan L Duncan Cancer Center).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA125123-12
Application #
9525818
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
12
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Mundt, Filip; Rajput, Sandeep; Li, Shunqiang et al. (2018) Mass Spectrometry-Based Proteomics Reveals Potential Roles of NEK9 and MAP2K4 in Resistance to PI3K Inhibition in Triple-Negative Breast Cancers. Cancer Res 78:2732-2746
Nair, Amritha; Chung, Hsiang-Ching; Sun, Tingting et al. (2018) Combinatorial inhibition of PTPN12-regulated receptors leads to a broadly effective therapeutic strategy in triple-negative breast cancer. Nat Med 24:505-511
Yu, Wangie; Chen, Yunyun; Dubrulle, Julien et al. (2018) Cisplatin generates oxidative stress which is accompanied by rapid shifts in central carbon metabolism. Sci Rep 8:4306
Singh, Ramesh; Karri, Dileep; Shen, Hong et al. (2018) TRAF4-mediated ubiquitination of NGF receptor TrkA regulates prostate cancer metastasis. J Clin Invest 128:3129-3143
Berntsson, Shala G; Merrell, Ryan T; Amirian, E Susan et al. (2018) Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case-control study. J Neurol 265:1432-1442
Chen, Fengju; Zhang, Yiqun; Gibbons, Don L et al. (2018) Pan-Cancer Molecular Classes Transcending Tumor Lineage Across 32 Cancer Types, Multiple Data Platforms, and over 10,000 Cases. Clin Cancer Res 24:2182-2193
Maldonado, Maria; Molfese, David L; Viswanath, Humsini et al. (2018) The habenula as a novel link between the homeostatic and hedonic pathways in cancer-associated weight loss: a pilot study. J Cachexia Sarcopenia Muscle 9:497-504
Richards, JoAnne S; Ren, Yi A; Candelaria, Nicholes et al. (2018) Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update. Endocr Rev 39:1-20
Kogiso, Mari; Qi, Lin; Braun, Frank K et al. (2018) Concurrent Inhibition of Neurosphere and Monolayer Cells of Pediatric Glioblastoma by Aurora A Inhibitor MLN8237 Predicted Survival Extension in PDOX Models. Clin Cancer Res 24:2159-2170
Takahashi, Hannah; Cornish, Alex J; Sud, Amit et al. (2018) Mendelian randomisation study of the relationship between vitamin D and risk of glioma. Sci Rep 8:2339

Showing the most recent 10 out of 991 publications