Accession Number:

ADA390721

Title:

Pathobiology of pp32 in Breast Cancer

Descriptive Note:

Annual rept. 1 Sep 1999-31 Aug 2000

Corporate Author:

JOHNS HOPKINS UNIV BALTIMORE MD SCHOOLOF MEDICINE

Personal Author(s):

Report Date:

2000-09-01

Pagination or Media Count:

8.0

Abstract:

Breast cancers differ from benign breast epithelium through prominent expression of oncogenic pp32 gene family members. Whereas benign breast epithelium predominantly expresses pp32, a tumor suppressor, breast cancers express pp32rl and pp32r2, which are oncogenic. The study purpose is to confirm and extend these preliminary results, to develop practical means to assay pp32 gene family members in clinical samples, and to determine the clinical significance of their presence in pre-invasive breast disease. The approved proposal encompassed four broad tasks 1 characterization of the pp32 expression phenotype of a larger sample of 40 breast cancers 2 development of a practical assay for altered pp32 transcripts in archival tissue 3determination of the association of specific pp32 variants in laser capture microdissected DCIS with invasion and with high-grade comedo DCIS and 4 application of the results in a retrospective study if 3 shows meaningful correlations to a population of patients with follow-up. During the reporting period, we recognized that microheterogeneity of pp32 gene family expression in tissue would best be assessed by an in situ hybridization method that would have better resolution than laser capture. This technically formidable task is now nearly complete and will facilitate rapid completion of the remaining aims.

Subject Categories:

  • Anatomy and Physiology
  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE