Sphingosine-1-Phosphate Receptor Subtype 3: A Novel Therapeutic Target of K-Ras Mutant Driven Non-Small Cell Lung Carcinoma

Abstract

This award aims to characterize the functional role of sphingosine-1-phosphate receptor subtype 3 (S1PR3) in oncogenic K-Ras mutant-mediated lung adenocarcinoma (AdC) progression, and to examine the novel therapeutic utility for K-Ras mutant-driven lung AdC by targeting S1PR3. There are two specific aims. Aim 1: We will use the LSL-K-RasG12D mouse model to investigate the role of S1PR3 in the development/maintenance of lung AdC.LSL-K-RasG12D will be bred with mice null for S1PR3. S1PR3-/-:LSL-K-RasG12D mice will be nasally instilled with adenoviral particle carrying Cre recombinase (Ad-Cre) to induce lung AdC. 3 months later, lung will be weighted, and lung tumor nodules will be quantitated. S1PR3 / :LSL-K-RasG12D mice will be used as a control. Aim 2: LSL-K-RasG12D mice will be instilled with Ad-Cre. Subsequently, TY-52156, a specific S1PR3 antagonist, will be i.p. injected every three days. Mice will be euthanized at 2 and 4 months. Hyperplasia of lung epithelial cells, development of lung adenomas and adenocarcinomas will be assessed. We have completed the animal treatments proposed in Aims 1 and 2. The collected mouse lung specimens are currently being analyzed.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2015
Accession Number
AD1007345

Entities

People

  • Menq-jer Lee

Organizations

  • Wayne State University

Tags

DTIC Thesaurus Topics

  • Acquisition
  • Adenocarcinoma
  • Biomedical Research
  • Cancer
  • Cells
  • Demographic Cohorts
  • Department Of Defense
  • Electronic Mail
  • Epithelial Cells
  • Hyperplasia
  • Information Operations
  • Lung Cancer
  • Neoplasms
  • Particles
  • Professional Development
  • Recombinases
  • Technology Transfer

Fields of Study

  • Biology
  • Chemistry

Readers

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  • Molecular Biology and Genetics
  • Toxicology/Environmental Toxicology