Breast cancer cells (BCC) frequently metastasize to the skeleton, where they lead to tumor-induced osteolysis and subsequent morbidity. Marc Lacroix has investigated the interrelationships between BCC and bone cells (osteoblasts, the bone-building cells, and osteoclasts, the bone-degrading cells). With colleagues, he discovered that BCC produce soluble factors increasing osteoclast activity, notably interleukin-11, the production of which is reduced by the cyclooxygenase inhibitor aspirin.[10][11][12] BCC also reduce the proliferation of osteoblasts and their production of collagen, the main protein component of bone.[13][14][15][non-primary sources needed] Lacroix also examined the response BCC to the anti-osteolytic agent calcitonin[16][17][non-primary sources needed]
The amount of data on breast cancer available for the scientific and medical community is growing rapidly. According to PubMed, a search engine offering access to the MEDLINEdatabase of citations and abstracts of biomedical research articles, 7918 papers containing the expression «breast cancer» were published in 2006. Their number was 3592 in 1996, 1455 in 1986 and only 626 in 1976. In general, the older information is overlaid by more recent data and forgotten to some extent. In 2004, Lacroix and colleagues collected and assembled data from hundreds of articles related to the biology, pathology and genetics of in situ, invasive and metastatic breast cancers. These papers were covering a time period of about 25 years. Lacroix et al. concluded that despite undergoing increasing genetic alteration, most individual breast cancers rather surprisingly maintain their phenotype when they evolve from in situ to the metastatic state.[27] This conclusion was in opposition to a progression model widely accepted at that time, which was suggesting that carcinomain situ could evolve into invasive carcinoma and subsequently produce metastases through an accumulation of molecular abnormalities possibly allowing extensive phenotype changes and subsequent gain of aggressiveness.
Bibliography: articles in scientific and medical journals (excerpt)
^Lacroix, M; Haibe-Kains B; Hennuy B; Laes JF; Lallemand F; Gonze I; Cardoso F; Piccart M; Leclercq G; Sotiriou C. (2004). "Gene regulation by phorbol 12-myristate 13-acetate in MCF-7 and MDA-MB-231, two breast cancer cell lines exhibiting highly different phenotypes". Oncology Reports. 12 (4): 701–707. doi:10.3892/or.12.4.701. PMID15375488. S2CID21227327.
^De Longueville F, Lacroix M, Barbuto AM, Bertholet V, Gallo D, Larsimont D, Marcq L, Zammatteo N, Boffe S, Leclercq G, Remacle J (2005). "Molecular characterization of breast cancer cell lines by a low-density microarray". International Journal of Oncology. 27 (4): 881–892. PMID16142302.
^Lacroix., M (2006). "Significance, detection and markers of disseminated breast cancer cells". Endocrine-Related Cancer. 13 (4): 1033–1067. doi:10.1677/ERC-06-0001. PMID17158753.
^Sotiriou C, Lacroix M, Lagneaux L, Berchem G, Body JJ (1999). "The aspirin metabolite salicylate inhibits breast cancer cells growth and their synthesis of the osteolytic cytokines interleukins-6 and-11". Anticancer Research. 19 (4B): 2997–3006. PMID10652584.
^Sotiriou, C; Lacroix M; Lespagnard L; Larsimont D; Paesmans M; Body JJ. (2001). "Interleukins-6 and-11 expression in primary breast cancer and subsequent development of bone metastases". Cancer Letters. 169 (1): 87–95. doi:10.1016/S0304-3835(01)00524-9. PMID11410329.
^Lacroix, M; Body JJ. (1997). "Regulation of c-fos and c-jun expression by calcitonin in human breast cancer cells". Calcified Tissue International. 60 (6): 513–519. doi:10.1007/s002239900273. PMID9164825. S2CID34337293.
^Borras, M; Lacroix M; Legros N; Leclercq G. (1997). "Estrogen receptor-negative/progesterone receptor-positive Evsa-T mammary tumor cells: a model for assessing the biological property of this peculiar phenotype of breast cancers". Cancer Letters. 120 (1): 23–30. doi:10.1016/S0304-3835(97)00285-1. PMID9570382.
^Rivas, A; Lacroix M; Olea-Serrano F; Laios I; Leclercq G; Olea N. (2002). "Estrogenic effect of a series of bisphenol analogues on gene and protein expression in MCF-7 breast cancer cells". Journal of Steroid Biochemistry and Molecular Biology. 82 (1): 45–53. doi:10.1016/S0960-0760(02)00146-2. PMID12429138. S2CID9619137.
^Lacroix, M; Leclercq G. (2004). "About GATA3, HNF3A, and XBP1, three genes co-expressed with the oestrogen receptor-α gene (ESR1) in breast cancer". Molecular and Cellular Endocrinology. 219 (1–2): 1–7. doi:10.1016/j.mce.2004.02.021. PMID15149721. S2CID38557047.
^Toillon RA, Magné N, Laïos I, Castadot P, Kinnaert E, Van Houtte P, Desmedt C, Leclercq G, Lacroix M (2007). "Estrogens decrease gamma-rays induced senescence and maintain cell cycle progression in breast cancer cells independently of p53". International Journal of Radiation Oncology, Biology, Physics. 67 (4): 1187–1200. doi:10.1016/j.ijrobp.2006.11.040. PMID17336220.
Leclercq G, Lacroix M, Seo HS, Larsimont D. "Mechanisms regulating oestrogen receptor α expression in breast cancer.", in "Molecular Mechanisms of Action of Steroid Hormone Receptors" 65–75 (2002). Editors: Marija Krstic-Demonacos & Constantinos Demonacos, Research Signpost Publishers, Trivandrum, India, ISBN81-7736-129-5, https://web.archive.org/web/20070217105555/http://www.ressign.com/
Sotiriou C, Desmedt C, Durbecq V, Dal Lago L, Lacroix M, Cardoso F, Piccart M. "Genomic and molecular classification of breast cancer.", in "Molecular Oncology of Breast Cancer" 81–95 (2004). Editors: Jeffrey S. Ross and Gabriel N. Hortobagy, Jones and Bartlett Publishers, 40 Tall Pine Drive, Sudbury, MA 01776 USA, ISBN0-7637-4810-2, http://www.jbpub.com/catalog/0763748102/table_of_contents.htm
Lacroix, Marc (2010). "MicroRNAs in Breast Cancer". In Martin E. Romero; Louis M. Dashek (eds.). Breast Cancer: Causes, Diagnosis and Treatment. Commack, N.Y: Nova Science Publishers. pp. 1–53. ISBN978-1-60876-463-1. Retrieved 29 November 2010.
Lacroix, Marc (2011). "MicroRNAs in Breast Cancer". In Eileen C. Roswell (ed.). Encyclopedia of Breast Cancer Research. Commack, N.Y: Nova Science Publishers. pp. ?. ISBN978-1-61324-388-6. Retrieved 3 March 2011.
Lacroix, Marc (2012). "MicroRNAs in Breast Cancer". In Gao Shi Tsai; Kong Ai Toh (eds.). Cancer Researcher Biographical Sketches and Research Summaries. Commack, N.Y: Nova Science Publishers. p. 171. ISBN978-1-61942-066-3. Retrieved 26 July 2013.