Lung cancer is the leading cause of cancer mortality worldwide causing more than 1.3 million deaths each year. Over ~700,000 of these victims succumb to lung cancers that have alterations in one of the genes encoding members of the Ubiquilin family (UBQLN). The UBQLN family of proteins consists of 5 family members (UBQLN1-4 and UBQLNL), which all contain ubiquitin-like (UBL) and ubiquitin-associated domains (UBA). There is very limited data on biological processes regulated by UBQLN proteins. A direct role for UBQLN proteins in human cancer has not previously been examined. The goal of this proposal is to understand how disruption of UBQLN1 or UBQLN2 contributes to the metastatic progression of human lung adenocarcinoma. The ultimate goal of this project is to identify the cellular processes altered specifically in cancers that harbor loss of UBQLN function. The preliminary data in this proposal are the first to suggest that UBQLN loss is capable of directly altering processes involved in metastatic progression of human lung cancer. We demonstrate that loss of UBQLN1 or UBQLN2 increases EMT, migration, and invasion of transformed and non-transformed lung epithelial cells and that UBQLN1 regulates multiple pathways known to be critical in human lung cancer, including IGF1R, mTOR, MYC and ERK. We propose to examine, in detail, how UBQLN1 and UBQLN2 regulate key steps of metastatic progression in vitro, as well as determine if UBQLN1 loss alters the in vivo kinetics of metastatic tumor progression. Importantly, we have observed that one allele of UBQLN1 or UBQLN2 is lost in over 50% of human lung adenocarcinomas. The data gained from this application will determine if cancers harboring altered UBQLN function represent a novel subset of lung cancers and if the expression of UBQLN family members can be used as a predictive biomarker to determine which patients are more likely to succumb to metastatic lung cancer. By understanding how alterations in UBQLN1 signaling contributes to metastatic progression we may be able to target these downstream pathways specifically in tumors with altered UBQLN1 function to block metastasis, thus potentially affecting millions of lung cancer patients in the coming decades.

Public Health Relevance

Lung cancer is a leading cause of cancer mortality throughout the world and adenocarcinoma sub-type of non-small cell lung cancer (NSCLC) now accounts for nearly 40% of all diagnosed lung cancer cases. This proposal seeks to advance our understanding of human lung cancer by examining how the novel family of proteins, the Ubiquilins (UBQLN), contributes to (NSCLC) in vitro and in vivo. Using cultured human adenocarcinoma cell lines, human lung adenocarcinoma cell lines, primary human lung cancer samples and oncogene-driven mouse models of NSCLC, we propose to characterize the role that UBQLN proteins plays in the genesis of human NSCLC.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA193220-05
Application #
9749963
Study Section
Tumor Progression and Metastasis Study Section (TPM)
Program Officer
Ault, Grace S
Project Start
2015-08-07
Project End
2020-07-31
Budget Start
2019-08-01
Budget End
2020-07-31
Support Year
5
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Louisville
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Barve, Aditya; Casson, Lavona; Krem, Maxwell et al. (2018) Comparative utility of NRG and NRGS mice for the study of normal hematopoiesis, leukemogenesis, and therapeutic response. Exp Hematol 67:18-31
Kurlawala, Zimple; Shah, Parag P; Shah, Charmi et al. (2017) The STI and UBA Domains of UBQLN1 Are Critical Determinants of Substrate Interaction and Proteostasis. J Cell Biochem 118:2261-2270
Shah, Parag P; Dupre, Tess V; Siskind, Leah J et al. (2017) Common cytotoxic chemotherapeutics induce epithelial-mesenchymal transition (EMT) downstream of ER stress. Oncotarget 8:22625-22639
Kurlawala, Zimple; Dunaway, Rain; Shah, Parag P et al. (2017) Regulation of insulin-like growth factor receptors by Ubiquilin1. Biochem J 474:4105-4118
Yadav, Sanjay; Singh, Nishant; Shah, Parag P et al. (2017) MIR155 Regulation of Ubiquilin1 and Ubiquilin2: Implications in Cellular Protection and Tumorigenesis. Neoplasia 19:321-332
Scherzer, Michael T; Waigel, Sabine; Donninger, Howard et al. (2015) Fibroblast-Derived Extracellular Matrices: An Alternative Cell Culture System That Increases Metastatic Cellular Properties. PLoS One 10:e0138065