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M.S. Orloff



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    P1.06 - Poster Session/ Screening and Early Detection (ID 218)

    • Event: WCLC 2015
    • Type: Poster
    • Track: Screening and Early Detection
    • Presentations: 1
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      P1.06-010 - Allelic Heterogeneity and Its Role in Identifying Non-Small Cell Lung Cancer Phenotypes (ID 2180)

      09:30 - 17:00  |  Author(s): M.S. Orloff

      • Abstract
      • Slides

      Background:
      More people die of lung cancer (LC) annually than of prostate, colon, and breast cancers combined, making it the leading cause of cancer-related mortality in the United States. LC can be divided into two main categories: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). NSCLC is the predominant LC category accounting for roughly 85% to 90% of all diagnosed LCs. NSCLC can be further subdivided into three main histological subtypes including adenocarcinoma, squamous cell carcinoma, and large cell carcinoma. Phenotypic characterization (i.e. histological features and LC subtypes) for NSCLC tissues remains a difficult task. Many studies have revealed certain genes that are associated with NSCLC; however, these genes cannot completely decipher between its varying phenotypes. CD36 is a biologically plausible candidate gene that is significantly under-expressed in NSCLC tissues compared to normal tissues. This differential expression is not observed in NSCLC tissue subtypes; however, significant differences in CD36 expression have been observed in NSCLC subtype-derived cell lines. Based on this previous expression data, we hypothesized that allelic heterogeneity within CD36 exons could disparately contribute to the development of NSCLC subtypes.

      Methods:
      To test this hypothesis, we obtained fresh-frozen LC tissues from the UAMS tissue bank and performed mutation screenings using Sanger sequencing methods and Mutation Surveyor software. Quantitative RT-PCR was performed on tissue mRNA and CD36 mRNA expression was normalized to HPRT1 (a housekeeping gene that is more stable in lung tissues) expression in the same samples. Genotype-specific CD36 expressions profiles were then identified and analyzed.

      Results:
      Several previously undiscovered variants were identified in Exon 4 of the CD36 gene. Two of these variants are associated with mRNA expression differences between the variant and wild-type genotypes that identify phenotypic heterogeneity. Adenocarcinoma samples with transcript harboring the first variant genotype overexpressed CD36 mRNA as compared to adenocarcinoma samples containing the wild-type genotype (p=0.013; N=37). In squamous cell carcinoma samples, there was no significant difference between samples with the first variant and wild-type (p=0.74; N=26). Squamous cell carcinoma samples with CD36 transcript harboring the second variant genotype was relatively under-expressed when compared to the squamous cell carcinoma samples with the wild-type genotype, though the comparison only approached significance at p=0.053 (N=37). A similar comparison in adenocarcinoma samples yielded non-significant results (p=0.59; N=25).

      Conclusion:
      Identification of NSCLC phenotypes is critical to treatment, but remains difficult with current histopathological methods. Our analysis of publicly available expression data has shown that probes used in global expression microarrays cannot completely and reliably distinguish between NSCLC phenotypes at the CD36 locus. We propose that allelic heterogeneity at the CD36 locus may alter array probe binding properties leading to inconsistent expression results. Our data has identified two previously undiscovered CD36 variants that may uniquely lead to altered CD36 mRNA expressions correlating to specific NSCLC subtypes. Hence, these results suggest that we may be able to accurately quantify transcripts associated with NSCLC subtypes using allele-specific probes.

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