TY - JOUR
T1 - Comparison of expression profiles of metastatic versus primary mammary tumors in MMTV-Wnt-1 and MMTV-Nue transgenic mice
AU - Huang, Shixia
AU - Chen, Yidong
AU - Podsypanina, Katrina
AU - Li, Yi
N1 - Funding Information:
Abbreviations: α-SMA, alpha-smooth muscle actin; ER, estrogen receptor; LRP, low-density lipoprotein receptor–related protein; MDS, multidimensional scaling; MMTV, mouse mammary tumor virus; mTOR, mammalian target of rapamycin Address all correspondence to: Shixia Huang, Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Room 130D, Houston, TX 77030. E-mail: [email protected] 1This work was supported in part by funds from the National Cancer Institute (R01CA113869-01 to Y.L.). Received 24 July 2007; Revised 15 November 2007; Accepted 16 November 2007 Copyright © 2008 Neoplasia Press, Inc. All rights reserved 1522-8002/08/$25.00 DOI 10.1593/neo.07637
PY - 2008/2
Y1 - 2008/2
N2 - Distant metastases of human breast cancers have been suggested to be more different from each other than from their respective primary tumors, based on expression profiling. The mechanism behind this lack of similarity between individual metastases is not known. We used cDNA microarrays to determine the expression profiles of pulmonary metastases and primary mammary tumors in two distinct transgenic models expressing either the Neu or the Wnt-1 oncogene from the mouse mammary tumor virus long terminal repeat (MMTV LTR). We found that pulmonary metastases are similar to each other and to their primary tumors within the same line. However, metastases arising in one transgenic mouse line are very different from either metastases or primary tumors arising in the other line. In addition, we found that, like their primary tumors, lung metastases in Wnt-1 transgenic mice harbor both epithelial and myoepithelial tumor cells and cells that express the putative progenitor cell marker keratin 6. Our data suggest that both gene expression profiles and cellular heterogeneity are preserved after breast cancer has spread to distant sites, and that metastases are similar to each other when their primary tumors were induced by the same oncogene and from the same subset of mammary cells.
AB - Distant metastases of human breast cancers have been suggested to be more different from each other than from their respective primary tumors, based on expression profiling. The mechanism behind this lack of similarity between individual metastases is not known. We used cDNA microarrays to determine the expression profiles of pulmonary metastases and primary mammary tumors in two distinct transgenic models expressing either the Neu or the Wnt-1 oncogene from the mouse mammary tumor virus long terminal repeat (MMTV LTR). We found that pulmonary metastases are similar to each other and to their primary tumors within the same line. However, metastases arising in one transgenic mouse line are very different from either metastases or primary tumors arising in the other line. In addition, we found that, like their primary tumors, lung metastases in Wnt-1 transgenic mice harbor both epithelial and myoepithelial tumor cells and cells that express the putative progenitor cell marker keratin 6. Our data suggest that both gene expression profiles and cellular heterogeneity are preserved after breast cancer has spread to distant sites, and that metastases are similar to each other when their primary tumors were induced by the same oncogene and from the same subset of mammary cells.
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U2 - 10.1593/neo.07637
DO - 10.1593/neo.07637
M3 - Article
C2 - 18283333
AN - SCOPUS:39049150399
SN - 1522-8002
VL - 10
SP - 118
EP - 124
JO - Neoplasia
JF - Neoplasia
IS - 2
ER -