Aurora a and B overexpression and centrosome amplification in early estrogen-induced tumor foci in the Syrian hamster kidney: implications for chromosomal instability, aneuploidy, and neoplasia

Cancer Res. 2007 Apr 1;67(7):2957-63. doi: 10.1158/0008-5472.CAN-06-3296.

Abstract

Estrogen-induced Syrian hamster tumors in the kidney represent a useful model to gain insight into the role of estrogens in oncogenic processes. We provided evidence that early tumor foci in the kidney arise from interstitial ectopic uterine-like germinal stem cells, and that early tumor foci and well-established tumors are highly aneuploid (92-94%). The molecular mechanisms whereby estrogens mediate this process are unclear. Here, we report that estrogen treatment induced significant increases in Aurora A protein expression (8.7-fold), activity (2.6-fold), mRNA (6.0-fold), and Aurora B protein expression (4.6-fold) in tumors, compared with age-matched cholesterol-treated kidneys. Immunohistochemistry revealed that this increase in Aurora A and B protein expression was essentially confined to cells within early and large tumor foci at 3.5 and 6 months of estrogen treatment, respectively. Upon estrogen withdrawal or coadministration of tamoxifen for 10 days, a 78% to 79% and 81% to 64% reduction in Aurora A and B expression, respectively, were observed in primary tumors compared with tumors continuously exposed to estrogens. These data indicate that overexpressed Aurora A and B in these tumors are under estrogen control via estrogen receptor alpha. Aurora A coenriched with the centrosome fraction isolated from tumors in the kidney. Centrosome amplification (number and area/cell) was detected in early tumor foci and large tumors but not in adjacent uninvolved or age-matched control kidneys. Taken together, these data indicate that persistent overexpression of Aurora A and B is under estrogen control, and is coincident with centrosome amplification, chromosomal instability, and aneuploidy, and represent an important mechanism driving tumorigenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aneuploidy*
  • Animals
  • Antineoplastic Agents, Hormonal / pharmacology
  • Aurora Kinases
  • Blotting, Western
  • Centrosome / enzymology*
  • Chromosomal Instability
  • Cricetinae
  • Estradiol
  • Kidney / drug effects
  • Kidney Neoplasms / chemically induced
  • Kidney Neoplasms / drug therapy
  • Kidney Neoplasms / enzymology*
  • Kidney Neoplasms / genetics*
  • Male
  • Mesocricetus
  • Orchiectomy
  • Protein Serine-Threonine Kinases / biosynthesis*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Tamoxifen / pharmacology

Substances

  • Antineoplastic Agents, Hormonal
  • RNA, Messenger
  • Tamoxifen
  • Estradiol
  • Aurora Kinases
  • Protein Serine-Threonine Kinases