Developing Personalized Medicine for Lung Cancer. The University of Texas SPORE in Lung Cancer represents a unique collaboration between the University of Texas Southwestern Medical Center (UTSW) and the University of Texas MD Anderson Cancer Center (MDACC) both of which have outstanding Strengths in lung cancer translational research. The overarching goal of the SPORE is to develop new experimental paradigms leading to personalized medicine approaches for lung cancer based on a molecular understanding of lung cancers in individual patients, and using this information to select the therapy (personalize) of each NSCLC patient's treatment. The SPORE builds on a 16 year productive history and incorporates recent advances made by SPORE investigators and others in lung cancer genomics, as well as important new advances in identifying and understanding lung cancer acquired vulnerabilities (synthetic lethalities). Together this will provide a more complete mechanistic understanding of the molecular findings so they can be applied to patients. These advances include novel approaches to functionally classify lung cancer by determining precisely the acquired vulnerabilities of each tumor, studying new molecular classifications of NSCLC related mRNA expression and DNA mutational clades and their functional characteristics, developing tools for CLIA certifiable molecular classification tests, preclinical model systems for testing the value of these new classification schemes, and a large legacy of molecular and clinical annotated datasets of lung cancers for retrospective analyses. The SPORE is composed of 4 projects: #1. Personalized medicine for NSCLC based on molecular portraits/clades; #2. Epidemiologic study of the role miR polymorphisms for predicting risk of lung cancer development and recurrence; #3. Therapeutic targeting of PI3K and MEK in mutant KRAS driven lung cancer for radiosensitization and blocking metastases; and #4. Therapeutic targeting of telomerase dependence on maintaining telomeres in lung cancer stem cells. In addition there are three cores: A. Administrative (including patient advocates), B. Molecular pathology, and C. Biostatistics-bioinformatics. The SPORE has some of the leading lung cancer translational investigators in the world in addition to a multidisciplinry group of clinical and laboratory scientists as well as a cadre of experienced patient advocates. The projects planned in this SPORE application will provide a new functional classification of lung cancer therapeutics, and the opportunity to change the face of NSCLC therapy.

Public Health Relevance

This SPORE in Lung Cancer assembles a multidisciplinary team of clinical and basic scientists from two leading lung cancer research institutions (UTSW and MDACC) to develop new ways to diagnose and treat lung cancer based on a rationale understanding of its molecular underpinnings and thus provide new 'personalized medicine' for lung cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
3P50CA070907-20S1
Application #
10019660
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Ujhazy, Peter
Project Start
1996-09-30
Project End
2020-08-31
Budget Start
2019-09-01
Budget End
2020-08-31
Support Year
20
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Pietanza, M Catherine; Waqar, Saiama N; Krug, Lee M et al. (2018) Randomized, Double-Blind, Phase II Study of Temozolomide in Combination With Either Veliparib or Placebo in Patients With Relapsed-Sensitive or Refractory Small-Cell Lung Cancer. J Clin Oncol 36:2386-2394
Abrams, Zachary B; Zucker, Mark; Wang, Min et al. (2018) Thirty biologically interpretable clusters of transcription factors distinguish cancer type. BMC Genomics 19:738
Tanaka, Ichidai; Sato, Mitsuo; Kato, Toshio et al. (2018) eIF2?, a subunit of translation-initiation factor EIF2, is a potential therapeutic target for non-small cell lung cancer. Cancer Sci 109:1843-1852
Huang, Fang; Ni, Min; Chalishazar, Milind D et al. (2018) Inosine Monophosphate Dehydrogenase Dependence in a Subset of Small Cell Lung Cancers. Cell Metab 28:369-382.e5
Robichaux, Jacqulyne P; Elamin, Yasir Y; Tan, Zhi et al. (2018) Mechanisms and clinical activity of an EGFR and HER2 exon 20-selective kinase inhibitor in non-small cell lung cancer. Nat Med 24:638-646
Pozo, Karine; Minna, John D; Johnson, Jane E (2018) Identifying a missing lineage driver in a subset of lung neuroendocrine tumors. Genes Dev 32:865-867
Fan, C-W; Yarravarapu, N; Shi, H et al. (2018) A synthetic combinatorial approach to disabling deviant Hedgehog signaling. Sci Rep 8:1133
Cascone, Tina; McKenzie, Jodi A; Mbofung, Rina M et al. (2018) Increased Tumor Glycolysis Characterizes Immune Resistance to Adoptive T Cell Therapy. Cell Metab 27:977-987.e4
Cascone, Tina; Gold, Kathryn A; Swisher, Stephen G et al. (2018) Induction Cisplatin Docetaxel Followed by Surgery and Erlotinib in Non-Small Cell Lung Cancer. Ann Thorac Surg 105:418-424
Ng, Patrick Kwok-Shing; Li, Jun; Jeong, Kang Jin et al. (2018) Systematic Functional Annotation of Somatic Mutations in Cancer. Cancer Cell 33:450-462.e10

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