Galectin-3 and L1 retrotransposons in human breast carcinomas

Pratima Nangia-Makker, Rebecca Sarvis, Daniel W. Visscher, Juliet Bailey-Penrod, Avraham Raz, Fazlul H. Sarkar

Research output: Contribution to journalArticle

38 Scopus citations

Abstract

Galectin-3 is a galactoside binding protein found at elevated levels in a wide variety of neoplastic cells and thought to be involved in cognitive cellular interactions during transformation and metastasis. Previously, we have shown that introduction of human galectin-3 (M(r) 31,000) cDNA into the human breast cancer cells BT-549 which are galectin-3 null and non-tumorigenic in nude mice resulted in the establishment of four galectin-3 expressing clones. Three of them acquired tumorigenicity when inoculated in the mammary fat pad of nude mice. Here, we questioned what is the molecular difference between the nude mouse tumorigenic and non-tumorigenic galectin-3 expressing BT-549 cell clones. Differential display analysis and Northern blotting revealed that, unlike the tumorigenic clones, neither the parental cells nor the non-tumorigenic clone expressed a 6.5 Kb transcript. A 607 bp PCR (polymerase chain reaction) product from the differentially displayed mRNA revealed a 93% sequence homology with the human L1 retrotransposon previously suggested to play a role in the pathobiology of some breast cancers. In addition, we show that the two gene products, i.e., galectin-3 and L1, are co-expressed in breast carcinoma specimens and in other nude mouse tumorigenic cell lines.

Original languageEnglish (US)
Pages (from-to)171-183
Number of pages13
JournalBreast Cancer Research and Treatment
Volume49
Issue number2
DOIs
StatePublished - Jun 29 1998

Keywords

  • Breast cancer
  • Galectin-3
  • Line 1 retrotransposon

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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    Nangia-Makker, P., Sarvis, R., Visscher, D. W., Bailey-Penrod, J., Raz, A., & Sarkar, F. H. (1998). Galectin-3 and L1 retrotransposons in human breast carcinomas. Breast Cancer Research and Treatment, 49(2), 171-183. https://doi.org/10.1023/A:1005913810250