Lung cancer is the leading cause of cancer related deaths in males and females in the United States. Surgical resection remains the only curative therapy for patients with non-small cell lung cancer (NSCLC). However, despite undergoing curative resection, a large percentage of patients with node negative NSCLC still develop recurrent disease. Thus, improvements in early detection are essential for improving the survival in patients with NSCLC. This study aims to use the power of molecular biology to develop and test new molecular markers for the early detection of NSCLC. As an interactive project, this study brings together promising new approaches from various investigators to develop new molecular markers garnished from the most promising areas of genetic research. Novel molecular markers will be developed by 1) the identification of tumor markers through serial analysis of gene expression (SAGE); 2) discovery of additional hypermethylated gene promoter regions for PCR based detection; and 3) identification of hypermutable sequences in mitochondrial DNA (a novel method of nucleic acid based detection). By integrating these promising approaches from diverse labs at John's Hopkins, we will develop a comprehensive profile of novel molecular markers. Using our available samples, we will be able to determine the timing of these molecular markers in lung cancer progression. We also have at our disposal a unique set of paired Bronchoalveolar Lavage (BAL) and serum samples from lung cancer patients allowing us to test newly identified markers outlined in this proposal. These critical resources will allow us to characterize newly developed markers for rapid translation in the clinical setting through the extended components of the early detection research network. Unlike the usual approach based on isolated investigators, this integrated approach will emphasize sharing of subjects, tissue samples, resources, technical expertise, and data analysis strategies. Our integrated effort will not only offer clinical direction for basic research efforts, but will also facilitate a direct translation of novel technology from the basic laboratory into clinical arena.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01CA084986-02S1
Application #
6333958
Study Section
Special Emphasis Panel (ZCA1 (O1))
Program Officer
Rosenfeld, Bobby
Project Start
1999-09-30
Project End
2004-08-31
Budget Start
2001-05-10
Budget End
2001-08-31
Support Year
2
Fiscal Year
2001
Total Cost
$156,807
Indirect Cost
Name
Johns Hopkins University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Pirini, Francesca; Noazin, Sassan; Jahuira-Arias, Martha H et al. (2017) Early detection of gastric cancer using global, genome-wide and IRF4, ELMO1, CLIP4 and MSC DNA methylation in endoscopic biopsies. Oncotarget 8:38501-38516
Guerrero-Preston, Rafael; White, James Robert; Godoy-Vitorino, Filipa et al. (2017) High-resolution microbiome profiling uncovers Fusobacterium nucleatum, Lactobacillus gasseri/johnsonii, and Lactobacillus vaginalis associated to oral and oropharyngeal cancer in saliva from HPV positive and HPV negative patients treated with surgery and Oncotarget 8:110931-110948
Guerrero-Preston, Rafael; Godoy-Vitorino, Filipa; Jedlicka, Anne et al. (2016) 16S rRNA amplicon sequencing identifies microbiota associated with oral cancer, human papilloma virus infection and surgical treatment. Oncotarget 7:51320-51334
Izumchenko, Evgeny; Chang, Xiaofei; Brait, Mariana et al. (2015) Targeted sequencing reveals clonal genetic changes in the progression of early lung neoplasms and paired circulating DNA. Nat Commun 6:8258
Izumchenko, Evgeny; Sun, Kai; Jones, Sian et al. (2015) Notch1 mutations are drivers of oral tumorigenesis. Cancer Prev Res (Phila) 8:277-286
Bateman, Nicholas W; Jaworski, Elizabeth; Ao, Wei et al. (2015) Elevated AKAP12 in paclitaxel-resistant serous ovarian cancer cells is prognostic and predictive of poor survival in patients. J Proteome Res 14:1900-10
Begum, Shahnaz; Hayashi, Masamichi; Ogawa, Takenori et al. (2015) An integrated genome-wide approach to discover deregulated microRNAs in non-small cell lung cancer: Clinical significance of miR-23b-3p deregulation. Sci Rep 5:13236
Kagohara, Luciane Tsukamoto; Schussel, Juliana L; Subbannayya, Tejaswini et al. (2015) Global and gene-specific DNA methylation pattern discriminates cholecystitis from gallbladder cancer patients in Chile. Future Oncol 11:233-49
Cherny, Nathan I; de Vries, Elisabeth G E; Emanuel, Linda et al. (2014) Words matter: distinguishing ""personalized medicine"" and ""biologically personalized therapeutics"". J Natl Cancer Inst 106:
Izumchenko, Evgeny; Chang, Xiaofei; Michailidi, Christina et al. (2014) The TGF?-miR200-MIG6 pathway orchestrates the EMT-associated kinase switch that induces resistance to EGFR inhibitors. Cancer Res 74:3995-4005

Showing the most recent 10 out of 144 publications