We had previously characterized a versatile transporter, DNP-SG ATPase in human tissues, which mediated the AlP-dependent transport of anionic glutathione-conjugates as well as doxorubicin (DOX). Studies in the currently funded project were aimed at structural and functional characterization of DNP-SG ATPase and immunologically related transport proteins with the overall objective of delineating their relevance to MDR. We are pleased to report successful cloning of DNP-SG AlPase, and its functional reconstitution in artificial proteoliposomes. Our studies show that DNP-SG ATPase is identical to RLIP76, a ral-binding GTPase activating effector protein with previously unknown function. Our studies demonstrated that DNP-SG ATPase RLIP76 is a 76 kDa precursor protein which gives rise to 5 major peptides which can reconstitute an AlP-dependent primary active DOX and glutathione conjugate transporter in artificial liposomes. RLIP76 over-expression confers a drug-accumulation defect and multidrug resistance when expressed in mammalian cells. Antibodies against RLIP76 inhibit DOX transport in lung cancer cells and markedly potentiate its cytotoxicity in a linear, concentration dependent manner at low concentrations. Comparison between SCLC and NSCLC shows that RLI76 is structurally and functionally distinct between SCLC and NSCLC: whereas SCLC express the wild-type RLIP76, NSCLC cells express a variant which has distinct proteolytic susceptibility, greater stability and significantly greater transport activity than RLIP76 from SCLC. Uptake of wild-type RLIP76-proteoliposomes by NSCLC confers a non-adherent morphology similar to that of SCLC. These observations lead us to hypothesize that RLIP76 is a multi-drug resistance-mediating precursor protein for an AlP-dependent transporter composed from its peptide fragments, that RLIP76 in NSCLC is more active than that present in SCLC, and that distinct nature/processing of its peptide fragments contributes to the observed differences in drug resistance and transport between SCLC and NSCLC. We propose to test our hypothesis through specific aims of 1) establishing that RLIP76 is a versatile AlP-dependent transporter of structurally diverse chemotherapeutic drugs, 2) demonstrating structure/function relationships for RLIP76 and its derived peptides, 3) comparing the function of RLIP76 as a drug and GS-E transporter in SCLC and NSCLC, 4) demonstrating that RLIP76 confers an MDR phenotype in lung cancer cells, and 5) demonstrating that limited tryptic peptides of RLIP76 can distinguish SCLC from NSCLC. These observations provide a potentially clinically relevant therapeutic target for lung cancer, and provide fundamental insight into the role in SCLC and NSCLC of drug-transport, signaling and GSH-linked biochemical pathways.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA077495-07
Application #
6704161
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Program Officer
Forry, Suzanne L
Project Start
1998-04-01
Project End
2006-02-28
Budget Start
2004-03-01
Budget End
2005-02-28
Support Year
7
Fiscal Year
2004
Total Cost
$245,680
Indirect Cost
Name
University of Texas Arlington
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
064234610
City
Arlington
State
TX
Country
United States
Zip Code
76019
Awasthi, Sanjay; Tompkins, Joshua; Singhal, Jyotsana et al. (2018) Rlip depletion prevents spontaneous neoplasia in TP53 null mice. Proc Natl Acad Sci U S A 115:3918-3923
Wurtzel, Jeremy G T; Lee, Seunghyung; Singhal, Sharad S et al. (2015) RLIP76 regulates Arf6-dependent cell spreading and migration by linking ARNO with activated R-Ras at recycling endosomes. Biochem Biophys Res Commun 467:785-91
Singhal, Sharad S; Singhal, Jyotsana; Figarola, James et al. (2015) RLIP76 Targeted Therapy for Kidney Cancer. Pharm Res 32:3123-36
Singhal, Sharad S; Singhal, Jyotsana; Figarola, James L et al. (2015) 2'-Hydroxyflavanone: A promising molecule for kidney cancer prevention. Biochem Pharmacol 96:151-8
Singhal, Sharad S; Singh, Sharda P; Singhal, Preeti et al. (2015) Antioxidant role of glutathione S-transferases: 4-Hydroxynonenal, a key molecule in stress-mediated signaling. Toxicol Appl Pharmacol 289:361-70
Figarola, James L; Singhal, Jyotsana; Rahbar, Samuel et al. (2014) LR-90 prevents methylglyoxal-induced oxidative stress and apoptosis in human endothelial cells. Apoptosis 19:776-88
Sahu, Mukesh; Sharma, Rajendra; Yadav, Sushma et al. (2014) Lens specific RLIP76 transgenic mice show a phenotype similar to microphthalmia. Exp Eye Res 118:125-34
Figarola, James Lester; Singhal, Preeti; Rahbar, Samuel et al. (2013) COH-SR4 reduces body weight, improves glycemic control and prevents hepatic steatosis in high fat diet-induced obese mice. PLoS One 8:e83801
Nagaprashantha, Lokesh Dalasanur; Talamantes, Tatjana; Singhal, Jyotsana et al. (2013) Proteomic analysis of signaling network regulation in renal cell carcinomas with differential hypoxia-inducible factor-2? expression. PLoS One 8:e71654
Yadav, Sushma; Sehrawat, Archana; Eroglu, Zeynep et al. (2013) Role of SMC1 in overcoming drug resistance in triple negative breast cancer. PLoS One 8:e64338

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