Abstract
Prostate cancer shows a propensity to form secondary tumours within the bone marrow. Such tumours are the major cause of mortality in this disease. We have developed an in vitro system to study the binding of prostate epithelial cells to bone marrow endothelium (BME) and stroma (BMS). The metastatic prostate cancer cell line, PC3 (derived from a bone metastasis), was seeded onto confluent layers of BME and its binding characteristics compared to human umbilical vein endothelial cells (HUVEC), lung endothelium (Hs888Lu) and BMS. The PC3 cell line showed significantly increased binding to BME (P< 0.05) compared to endothelium derived from HUVEC and lung or BMS with maximal binding occurring at 1 h. Following pre-incubation with a β1 integrin antibody PC3 binding to BME was inhibited by 64% (P< 0.001). Antibodies directed against the integrins β4, α2, α4, α5 and the cellular adhesion molecules P-selectin, CD31, VCAM-1 and sialy Lewis X showed no effect on blocking PC3 binding. Primary prostatic epithelial cells from both malignant (n = 11) and non-malignant tissue (n = 11) also demonstrated equivalent levels of increased adhesion to BME and BMS compared to HUVEC, peaking at 24 h. Further studies examined the invasive ability of prostate epithelial cells in response to bone marrow endothelium using Matrigel invasion chamber assays. In contrast to the previous results, malignant cells showed an increase (1000 fold) in invasive ability, whilst non-malignant prostate epithelia did not respond. We have shown that both malignant and non-malignant prostate epithelial cells can bind at equivalent levels and preferentially to primary human bone marrow endothelium in comparison to controls. However, only malignant prostate epithelia show increased invasive ability in response to BME. © 2001 Cancer Research Campaign www.bjcancer.com
Keywords: prostate cancer, prostate epithelia, bone marrow endothelium, metastasis
Full Text
The Full Text of this article is available as a PDF (314.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alby L., Auerbach R. Differential adhesion of tumor cells to capillary endothelial cells in vitro. Proc Natl Acad Sci U S A. 1984 Sep;81(18):5739–5743. doi: 10.1073/pnas.81.18.5739. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arcangeli G., Micheli A., Verna L., Saracino B., Arcangeli G., Giovinazzo G., D'Angelo L., Pansadoro V., Sternberg C. N. Prognostic impact of transurethral resection on patients irradiated for localized prostate cancer. Radiother Oncol. 1995 May;35(2):123–128. doi: 10.1016/0167-8140(95)01527-n. [DOI] [PubMed] [Google Scholar]
- Auerbach R., Lu W. C., Pardon E., Gumkowski F., Kaminska G., Kaminski M. Specificity of adhesion between murine tumor cells and capillary endothelium: an in vitro correlate of preferential metastasis in vivo. Cancer Res. 1987 Mar 15;47(6):1492–1496. [PubMed] [Google Scholar]
- Bonkhoff H., Stein U., Remberger K. Differential expression of alpha 6 and alpha 2 very late antigen integrins in the normal, hyperplastic, and neoplastic prostate: simultaneous demonstration of cell surface receptors and their extracellular ligands. Hum Pathol. 1993 Mar;24(3):243–248. doi: 10.1016/0046-8177(93)90033-d. [DOI] [PubMed] [Google Scholar]
- Dejana E., Martin-Padura I., Lauri D., Bernasconi S., Bani M. R., Garofalo A., Giavazzi R., Magnani J., Mantovani A., Menard S. Endothelial leukocyte adhesion molecule-1-dependent adhesion of colon carcinoma cells to vascular endothelium is inhibited by an antibody to Lewis fucosylated type I carbohydrate chain. Lab Invest. 1992 Mar;66(3):324–330. [PubMed] [Google Scholar]
- Fidler I. J., Gersten D. M., Hart I. R. The biology of cancer invasion and metastasis. Adv Cancer Res. 1978;28:149–250. doi: 10.1016/s0065-230x(08)60648-x. [DOI] [PubMed] [Google Scholar]
- Galasko C. S. Bone metastases studied in experimental animals. Clin Orthop Relat Res. 1981 Mar-Apr;(155):269–285. [PubMed] [Google Scholar]
- George N. J. Natural history of localised prostatic cancer managed by conservative therapy alone. Lancet. 1988 Mar 5;1(8584):494–497. doi: 10.1016/s0140-6736(88)91294-9. [DOI] [PubMed] [Google Scholar]
- Honn K. V., Tang D. G. Adhesion molecules and tumor cell interaction with endothelium and subendothelial matrix. Cancer Metastasis Rev. 1992 Nov;11(3-4):353–375. doi: 10.1007/BF01307187. [DOI] [PubMed] [Google Scholar]
- Iwai K., Ishikura H., Kaji M., Sugiura H., Ishizu A., Takahashi C., Kato H., Tanabe T., Yoshiki T. Importance of E-selectin (ELAM-1) and sialyl Lewis(a) in the adhesion of pancreatic carcinoma cells to activated endothelium. Int J Cancer. 1993 Jul 30;54(6):972–977. doi: 10.1002/ijc.2910540618. [DOI] [PubMed] [Google Scholar]
- Jackson C. J., Garbett P. K., Nissen B., Schrieber L. Binding of human endothelium to Ulex europaeus I-coated Dynabeads: application to the isolation of microvascular endothelium. J Cell Sci. 1990 Jun;96(Pt 2):257–262. doi: 10.1242/jcs.96.2.257. [DOI] [PubMed] [Google Scholar]
- Jacobs S. C. Spread of prostatic cancer to bone. Urology. 1983 Apr;21(4):337–344. doi: 10.1016/0090-4295(83)90147-4. [DOI] [PubMed] [Google Scholar]
- Jensen O. M., Estève J., Møller H., Renard H. Cancer in the European Community and its member states. Eur J Cancer. 1990;26(11-12):1167–1256. doi: 10.1016/0277-5379(90)90278-2. [DOI] [PubMed] [Google Scholar]
- Jørgensen T., Berner A., Kaalhus O., Tveter K. J., Danielsen H. E., Bryne M. Up-regulation of the oligosaccharide sialyl LewisX: a new prognostic parameter in metastatic prostate cancer. Cancer Res. 1995 May 1;55(9):1817–1819. [PubMed] [Google Scholar]
- Kannagi R. Carbohydrate-mediated cell adhesion involved in hematogenous metastasis of cancer. Glycoconj J. 1997 Aug;14(5):577–584. doi: 10.1023/a:1018532409041. [DOI] [PubMed] [Google Scholar]
- Kostenuik P. J., Sanchez-Sweatman O., Orr F. W., Singh G. Bone cell matrix promotes the adhesion of human prostatic carcinoma cells via the alpha 2 beta 1 integrin. Clin Exp Metastasis. 1996 Jan;14(1):19–26. doi: 10.1007/BF00157682. [DOI] [PubMed] [Google Scholar]
- Lang S. H., Clarke N. W., George N. J., Allen T. D., Testa N. G. Interaction of prostate epithelial cells from benign and malignant tumor tissue with bone-marrow stroma. Prostate. 1998 Feb 15;34(3):203–213. doi: 10.1002/(sici)1097-0045(19980215)34:3<203::aid-pros8>3.0.co;2-i. [DOI] [PubMed] [Google Scholar]
- Lang S. H., Clarke N. W., George N. J., Testa N. G. Primary prostatic epithelial cell binding to human bone marrow stroma and the role of alpha2beta1 integrin. Clin Exp Metastasis. 1997 May;15(3):218–227. doi: 10.1023/a:1018465213641. [DOI] [PubMed] [Google Scholar]
- Lehr J. E., Pienta K. J. Preferential adhesion of prostate cancer cells to a human bone marrow endothelial cell line. J Natl Cancer Inst. 1998 Jan 21;90(2):118–123. doi: 10.1093/jnci/90.2.118. [DOI] [PubMed] [Google Scholar]
- Majuri M. L., Mattila P., Renkonen R. Recombinant E-selectin-protein mediates tumor cell adhesion via sialyl-Le(a) and sialyl-Le(x). Biochem Biophys Res Commun. 1992 Feb 14;182(3):1376–1382. doi: 10.1016/0006-291x(92)91885-t. [DOI] [PubMed] [Google Scholar]
- Masek L. C., Sweetenham J. W. Isolation and culture of endothelial cells from human bone marrow. Br J Haematol. 1994 Dec;88(4):855–865. doi: 10.1111/j.1365-2141.1994.tb05128.x. [DOI] [PubMed] [Google Scholar]
- McCarthy S. A., Kuzu I., Gatter K. C., Bicknell R. Heterogeneity of the endothelial cell and its role in organ preference of tumour metastasis. Trends Pharmacol Sci. 1991 Dec;12(12):462–467. doi: 10.1016/0165-6147(91)90637-8. [DOI] [PubMed] [Google Scholar]
- Merwin J. R., Madri J. A., Lynch M. Cancer cell binding to E-selectin transfected human endothelia. Biochem Biophys Res Commun. 1992 Nov 30;189(1):315–323. doi: 10.1016/0006-291x(92)91560-d. [DOI] [PubMed] [Google Scholar]
- Murant S. J., Handley J., Stower M., Reid N., Cussenot O., Maitland N. J. Co-ordinated changes in expression of cell adhesion molecules in prostate cancer. Eur J Cancer. 1997 Feb;33(2):263–271. doi: 10.1016/s0959-8049(96)00418-2. [DOI] [PubMed] [Google Scholar]
- Mårtensson S., Bigler S. A., Brown M., Lange P. H., Brawer M. K., Hakomori S. Sialyl-Lewis(x) and related carbohydrate antigens in the prostate. Hum Pathol. 1995 Jul;26(7):735–739. doi: 10.1016/0046-8177(95)90220-1. [DOI] [PubMed] [Google Scholar]
- Nagle R. B., Knox J. D., Wolf C., Bowden G. T., Cress A. E. Adhesion molecules, extracellular matrix, and proteases in prostate carcinoma. J Cell Biochem Suppl. 1994;19:232–237. [PubMed] [Google Scholar]
- Nicolson G. L., Winkelhake J. L. Organ specificity of blood-borne tumour metastasis determined by cell adhesion? Nature. 1975 May 15;255(5505):230–232. doi: 10.1038/255230a0. [DOI] [PubMed] [Google Scholar]
- Paget S. The distribution of secondary growths in cancer of the breast. 1889. Cancer Metastasis Rev. 1989 Aug;8(2):98–101. [PubMed] [Google Scholar]
- Price E. A., Coombe D. R., Murray J. C. beta-1 Integrins mediate tumour cell adhesion to quiescent endothelial cells in vitro. Br J Cancer. 1996 Dec;74(11):1762–1766. doi: 10.1038/bjc.1996.627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rokhlin O. W., Cohen M. B. Expression of cellular adhesion molecules on human prostate tumor cell lines. Prostate. 1995 Apr;26(4):205–212. doi: 10.1002/pros.2990260406. [DOI] [PubMed] [Google Scholar]
- Shevrin D. H., Gorny K. I., Kukreja S. C. Patterns of metastasis by the human prostate cancer cell line PC-3 in athymic nude mice. Prostate. 1989;15(2):187–194. doi: 10.1002/pros.2990150212. [DOI] [PubMed] [Google Scholar]
- Soligo D., Schiró R., Luksch R., Manara G., Quirici N., Parravicini C., Lambertenghi Deliliers G. Expression of integrins in human bone marrow. Br J Haematol. 1990 Nov;76(3):323–332. doi: 10.1111/j.1365-2141.1990.tb06363.x. [DOI] [PubMed] [Google Scholar]
- Takada A., Ohmori K., Yoneda T., Tsuyuoka K., Hasegawa A., Kiso M., Kannagi R. Contribution of carbohydrate antigens sialyl Lewis A and sialyl Lewis X to adhesion of human cancer cells to vascular endothelium. Cancer Res. 1993 Jan 15;53(2):354–361. [PubMed] [Google Scholar]
- Tanaka Y., Albelda S. M., Horgan K. J., van Seventer G. A., Shimizu Y., Newman W., Hallam J., Newman P. J., Buck C. A., Shaw S. CD31 expressed on distinctive T cell subsets is a preferential amplifier of beta 1 integrin-mediated adhesion. J Exp Med. 1992 Jul 1;176(1):245–253. doi: 10.1084/jem.176.1.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trikha M., Raso E., Cai Y., Fazakas Z., Paku S., Porter A. T., Timar J., Honn K. V. Role of alphaII(b)beta3 integrin in prostate cancer metastasis. Prostate. 1998 May 15;35(3):185–192. doi: 10.1002/(sici)1097-0045(19980515)35:3<185::aid-pros4>3.0.co;2-g. [DOI] [PubMed] [Google Scholar]
- Zaifert K., Cohen M. C. COLO 205 utilizes E-selectin to adhere to human endothelium. Clin Immunol Immunopathol. 1993 Jul;68(1):51–56. doi: 10.1006/clin.1993.1094. [DOI] [PubMed] [Google Scholar]
- Zetter B. R. The cellular basis of site-specific tumor metastasis. N Engl J Med. 1990 Mar 1;322(9):605–612. doi: 10.1056/NEJM199003013220907. [DOI] [PubMed] [Google Scholar]
- Zheng D. Q., Woodard A. S., Fornaro M., Tallini G., Languino L. R. Prostatic carcinoma cell migration via alpha(v)beta3 integrin is modulated by a focal adhesion kinase pathway. Cancer Res. 1999 Apr 1;59(7):1655–1664. [PubMed] [Google Scholar]
