4.5 Article

Variation in genes coding for AMP-activated protein kinase (AMPK) and breast cancer risk in the European Prospective Investigation on Cancer (EPIC)

Journal

BREAST CANCER RESEARCH AND TREATMENT
Volume 127, Issue 3, Pages 761-767

Publisher

SPRINGER
DOI: 10.1007/s10549-010-1269-1

Keywords

AMP-activated protein kinase; Breast cancer; Cancer susceptibility; Body-mass index

Categories

Funding

  1. US Army Medical Research and Material Command [W81XWH-04-1-0271]
  2. European Commission (SANCO)
  3. Ligue contre le Cancer
  4. Institut Gustave Roussy
  5. Mutuelle Generale de l'Education Nationale
  6. Institut National de la Sante et de la Recherche Medicale (INSERM)
  7. German Cancer Aid
  8. German Cancer Research Center
  9. German Federal Ministry of Education and Research
  10. Danish Cancer Society
  11. Spanish Ministry of Health
  12. Cancer Research UK
  13. Medical Research Council, UK
  14. Hellenic Ministry of Health and Social Solidarity
  15. Stavros Niarchos Foundation
  16. Hellenic Health Foundation
  17. Italian Association for Research on Cancer
  18. Italian National Research Council
  19. Dutch Ministry of Public Health, Welfare and Sports (VWS)
  20. Dutch Ministry of Health
  21. Netherlands Cancer Registry (NKR)
  22. LK Research Funds
  23. Dutch Prevention Funds
  24. Dutch ZON (Zorg Onderzoek Nederland)
  25. World Cancer Research Fund (WCRF) (The Netherlands)
  26. Statistics Netherlands
  27. Swedish Cancer Society
  28. Swedish Scientific Council
  29. Regional Government of Skane, Sweden
  30. Norwegian Cancer Society
  31. Medical Research Council [G1000143, G0401527, MC_U106179471] Funding Source: researchfish

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AMP-activated protein kinase (AMPK) is an energy sensing/signalling intracellular protein which is activated by an increase in the cellular AMP:ATP ratio after ATP depletion. Once activated, AMPK inhibits fatty acid synthesis and the Akt-mTOR pathway, and activates the p53-p21 axis. All these molecular mechanisms are thought to play a key role in breast carcinogenesis. We investigated the genetic variability of four genes encoding AMPK (PRKAA1, PRKAA2, PRKAB1 and PRKAB2). Using a tagging approach and selecting SNPs we covered all the common genetic variation of these genes. We tested association of tagging SNPs in our four candidate genes with breast cancer (BC) risk in a study of 1340 BC cases and 2536 controls nested into the European Prospective Investigation into Cancer and Nutrition (EPIC). Given the relevance of AMPK on fatty acid synthesis and the importance of body fatness as a BC risk factor, we tested association of SNPs and body-mass index as well. We observed no statistically significant association between the SNPs in the PRKAs genes and BC risk and BMI after correction for multiple testing.

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