From Wikipedia, the free encyclopedia
Marc Lacroix is a biochemist (educated at University of Liège) and a researcher (b: April 28,
1963 in Verviers, Wallonia, Belgium) who specializes in breast cancer biology, metastasis and therapy.[1][2][3][4][5][6][7][8][9]
He works at Institut Jules Bordet (Brussels, Belgium).
Earlier
work
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].
Marc Lacroix also examined the response BCC to the anti-osteolytic
agent calcitonin [16][17]
In close collaboration with Prof. Guy Leclercq (Institut Jules
Bordet, Belgium), Marc Lacroix has studied various aspects of estrogen
receptor biology, ligand-binding and transcriptional activity,
and life-cycle.[18][19][20][21][22][23][24][25][26]
Recent
work
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 MEDLINE database 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 overlayed 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 carcinoma in 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)
- ^ Siwek, B; Larsimont D, Lacroix M, Body JJ,
(1998). "Establishment and characterization of three new
breast-cancer cell lines". International Journal of Cancer
76: 677 – 683. doi:10.1002/(SICI)1097-0215(19980529)76:5<677::AID-IJC11>3.0.CO;2-1.
PMID 9610725.
- ^ Lacroix, M; Zammatteo N, Remacle J,
Leclercq G. (2002). "A low-density DNA microarray for analysis of markers in breast
cancer". International Journal of Biological Markers
17: 5 – 23. PMID 11936587.
- ^ Lacroix, M; Leclercq G. (2004). "Relevance
of breast cancer cell lines as models for breast tumours: an
update". Breast
Cancer Research and Treatment 83: 249 –
289. doi:10.1023/B:BREA.0000014042.54925.cc. PMID 14758095.
- ^ 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: 701 – 707. PMID 15375488.
- ^ Lacroix, M; Leclercq G, on behalf of
BreastMed Consortium. (2005). "The "portrait" of hereditary breast
cancer". Breast
Cancer Research and Treatment 89: 297 –
304. doi:10.1007/s10549-004-2172-4. PMID 15754129.
- ^ De Longueville, F; Lacroix M (co-first
author), 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: 881 – 892. PMID 16142302.
- ^ Lacroix, M; Toillon RA, Leclercq G.
(2006). "P53 and breast cancer, an update". Endocrine-Related
Cancer 13: 293 – 325. doi:10.1677/erc.1.01172. PMID 16728565.
- ^ Lacroix., M (2006). "Significance,
detection and markers of disseminated breast cancer cells".
Endocrine-Related Cancer 13: 1033–1067.
doi:10.1677/ERC-06-0001. PMID 17158753.
- ^ Lacroix., M (2008). "Persistent use of
"false" cell lines". International Journal of Cancer
122: 1 – 4. doi:10.1002/ijc.23233.
PMID 17960586.
- ^ Lacroix, M; Siwek B, Marie PJ, Body JJ.
(1998). "Production and regulation of interleukin-11 by breast cancer
cells". Cancer Letters 127: 29 – 35. doi:10.1016/S0304-3835(97)00542-9. PMID 9619855.
- ^ Sotiriou, C; Lacroix M (co-first author),
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: 2997 –
3006. PMID 10652584.
- ^ 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: 87
– 95. doi:10.1016/S0304-3835(01)00524-9. PMID 11410329.
- ^ Lacroix, M; Siwek B, Body JJ. (1996).
"Effects of secretory products of breast cancer cells on osteoblast-like cells".
Breast
Cancer Research and Treatment 38: 209 –
216. doi:10.1007/BF01806675. PMID 8861839.
- ^ Siwek, B; Lacroix M, DePollak C, Marie P,
Body JJ. (1997). "Secretory products of breast cancer cells
specifically affect human osteoblastic cells: Partial
characterization of active factors". Journal of Bone and
Mineral Research 12: 552 – 560. doi:10.1359/jbmr.1997.12.4.552. PMID 9101366.
- ^ Lacroix, M; Lacroix M, Marie PJ, Body JJ.
(2000). "Protein production by osteoblasts: modulation by breast
cancer cell-derived factors". Breast
Cancer Research and Treatment 61: 59 –
67. doi:10.1023/A:1006408916224. PMID 10930090.
- ^ Lacroix, M; Body JJ. (1997). "Regulation
of c-fos and c-jun expression by
calcitonin in human
breast cancer cells". Calcified Tissue International
60: 513 – 519. doi:10.1007/s002239900273. PMID 9164825.
- ^ Lacroix, M; Siwek B, Body JJ. (1998).
"Breast cancer cell response to calcitonin: Modulation by growth-regulating
agents". European Journal of Pharmacology
344: 279 – 286. doi:10.1016/S0014-2999(97)01578-1. PMID 9600664.
- ^ Jin, L; Borras M, Lacroix M, Legros N,
Leclercq G. (1995). "Antiestrogenic activity of 2 11-beta-estradiol
derivatives on MCF-7 breast cancer cells". Steroids
60: 512 – 518. doi:10.1016/0039-128X(95)00079-6. PMID 8539793.
- ^ 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: 23 –
30. doi:10.1016/S0304-3835(97)00285-1. PMID 9570382.
- ^ Maaroufi, Y; Lacroix M, Lespagnard L,
Journe F, Larsimont D, Leclercq G. (2000). "Estrogen
receptor of primary breast cancers: evidence for intracellular
proteolysis". Breast Cancer Research 2:
444 – 454. doi:10.1186/bcr92. PMID 11056692.
- ^ Lacroix, M; Querton G, Hennebert P,
Larsimont D, Leclercq G. (2001). "Estrogen receptor analysis in
primary breast tumors by ligand-binding assay, immmocytochemical
assay, and northern blot: a comparison". Breast
Cancer Research and Treatment 67: 263 –
271. doi:10.1023/A:1017946810277. PMID 11561772.
- ^ 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: 45 – 53. doi:10.1016/S0960-0760(02)00146-2. PMID 12429138.
- ^ Lacroix, M; Leclercq G. (2004). "About
GATA3, HNF3A, and XBP1, three genes co-expressed with the oestrogen
receptor-alpha gene (ESR1) in breast cancer". Molecular and
Cellular Endocrinology 219: 1 – 7. doi:10.1016/j.mce.2004.02.021. PMID 15149721.
- ^ Toillon, RA; Magné N, Laios I, Lacroix M,
Duvillier H, Lagneaux L, Devriendt D, Van Houtte P, Leclercq G.
(2005). "Interaction between estrogen receptor alpha, ionizing
radiation and (anti-) estrogens in breast cancer cells". Breast
Cancer Research and Treatment 93: 207 –
215. doi:10.1007/s10549-005-5148-0. PMID 16136271.
- ^ Leclercq, G; Lacroix M, Laïos I, Laurent
G. (2006). "Estrogen receptor alpha: impact of ligands on
intracellular shuttling and turnover rate in breast cancer cells".
Current Cancer Drug Targets 6: 39 – 64.
doi:10.2174/156800906775471716. PMID 16475975.
- ^ 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: 1187 – 1200. PMID 17336220.
- ^ Lacroix, M; Toillon RA, Leclercq G.
(2004). "Stable 'portrait' of breast tumors during progression:
data from biology, pathology and genetics". Endocrine-Related
Cancer 11: 497 – 522. doi:10.1677/erc.1.00758. PMID 15369451.
Bibliography:
invited chapters in thematic books
- Leclercq G, Lacroix M, Seo HS, Larsimont D. "Mechanisms
regulating oestrogen receptor alpha 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, ISBN
81-7736-129-5, 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,
ISBN 0-76374-810-2, http://www.jbpub.com/catalog/0763748102/table_of_contents.htm
Bibliography: books
- Lacroix M. Tumor suppressor genes in breast cancer (2008). Nova
Science Publishers, Inc, 400 Oser Ave, Ste 1600, Hauppauge, NY
11788-3635 USA, https://www.novapublishers.com/catalog/product_info.php?products_id=6866,
ISBN 978-1-60456-326-9
- Lacroix M. Molecular therapy of breast cancer: classicism meets
modernity (2009). Nova Science Publishers, Inc, 400 Oser Ave, Ste
1600, Hauppauge, NY 11788-3635 USA, https://www.novapublishers.com/catalog/product_info.php?products_id=10042,
ISBN 978-1-60741-593-0
References
Over the years, Marc Lacroix has been refereeing for several
international scientific and clinical journals:
External
links