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Molecular Biology Reports

, Volume 39, Issue 12, pp 10131–10137 | Cite as

TGF-β polymorphism and its expression correlated with CXCR4 expression in human breast cancer

  • Julie Massayo Maeda Oda
  • Karen Brajão de Oliveira
  • Roberta Losi Guembarovski
  • Kalil William Alves de Lima
  • Ana Cristina da Silva do Amaral Herrera
  • Alda Losi Guembarovski
  • Walter Jorge Sobrinho
  • Daniela Rudgeri Derossi
  • Maria Angelica Ehara Watanabe
Article

Abstract

The role of chemokines and the growth factors has been extensively analyzed both in cancer risk and tumor progression. The transforming growth factor beta (TGF-β) and chemokine (C-X-C motif) receptor 4 (CXCR4) genes are implicated in several diseases, including breast cancer. Genomic DNA was obtained from 21 samples of peripheral blood or from normal tissue, previously fixed in formalin and embedded in paraffin for TGF-β T869C polymorphism analyses. Total cellular RNA was extracted from the same 21 patients, but from fresh tissue (tumor and adjacent healthy from the same breast) for expression analysis by Real Time PCR. No significant differences were observed in genotype distribution according to clinicopathological characteristics. Transforming growth factor beta (TGF-β) mRNA expression was assessed according to T869C polymorphism and CC patients presented a higher TGF-β expression but not significant when compared to other genotypes (p = 0.064). A positive correlation was observed in relative mRNA expressions of CXCR4 and TGF-β (p = 0.020). It is known that overexpression of TGF-β by both tumor and stromal tissue can facilitate the development of metastases, mainly by TGF-β stimulated angiogenesis and increased tumor cell motility. Our findings suggested a role of these genes as progression markers for breast carcinoma.

Keywords

Breast cancer TGF-β CXCR4 qRT-PCR 

Notes

Acknowledgments

The authors would like to acknowledge the volunteers who made this study possible and the Cancer Hospital of Londrina, Micropar and Preventivo Histopathological Laboratories, Londrina, PR, Brazil. This study was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Fundação Araucária-Programa Pesquisa para o SUS: gestão compartilhada em saúde (PPSUS) and the Londrina State University Graduate Coordination (PROPPG-UEL). The authors would like to express their gratitude to GENOPAR for supplying laboratory equipment. The entire article was revised by Adrienne Toledo, a British-born scientific editor.

Conflict of interest

The authors declared that they had no conflict of interest related to the publication of this manuscript.

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Copyright information

© Springer Science+Business Media B.V. 2012

Authors and Affiliations

  • Julie Massayo Maeda Oda
    • 1
  • Karen Brajão de Oliveira
    • 1
  • Roberta Losi Guembarovski
    • 1
  • Kalil William Alves de Lima
    • 1
  • Ana Cristina da Silva do Amaral Herrera
    • 1
    • 2
  • Alda Losi Guembarovski
    • 3
    • 4
  • Walter Jorge Sobrinho
    • 5
  • Daniela Rudgeri Derossi
    • 2
    • 3
  • Maria Angelica Ehara Watanabe
    • 1
  1. 1.Department of Pathological Sciences, Biological Sciences CenterState University of LondrinaLondrinaBrazil
  2. 2.Center of Cancer Research on Londrina Cancer HospitalLondrina Cancer HospitalLondrinaBrazil
  3. 3.Laboratory of Pathology, Healthy Sciences CenterState University of LondrinaLondrinaBrazil
  4. 4.Laboratory of Applied PathologyMICROPARLondrinaBrazil
  5. 5.Gineco-Med Clinical of MastologyLondrinaBrazil

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