Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

British Journal of Cancer
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. british journal of cancer
  3. regular article
  4. article
Development and characterization of a tamoxifen-resistant breast carcinoma xenograft
Download PDF
Download PDF
  • Regular Article
  • Open access
  • Published: 04 May 2000

Development and characterization of a tamoxifen-resistant breast carcinoma xenograft

  • H Naundorf1,
  • M Becker1,
  • A E Lykkesfeldt2,
  • B Elbe1,
  • C Neumann1,
  • B Büttner1 &
  • …
  • I Fichtner1 

British Journal of Cancer volume 82, pages 1844–1850 (2000)Cite this article

  • 1506 Accesses

  • 19 Citations

  • Metrics details

This article has been updated

Abstract

A human tamoxifen-resistant mammary carcinoma, MaCa 3366/TAM, originating from a sensitive parental xenograft 3366 was successfully established by treatment of tumour-bearing nude mice with 1–50 mg kg–1 tamoxifen for 3 years during routine passaging. Both tumours did not differ significantly in OR- and PR-positivity, however, when compared with the sensitive tumour line, the mean OR content of the TAM-resistant subline is slightly lower. An OR-upregulation following withdrawal of oestradiol treatment was observed in the parental tumours but not in the resistant xenografts. Following long-term treatment with tamoxifen, the histological pattern of the breast carcinoma changed. The more differentiated structures being apparent after treatment with 17β-oestradiol in the original 3366 tumour were not induced in the resistant line. Tamoxifen failed to induce a tumour growth inhibition in comparison to the tamoxifen-sensitive line. The pure anti-oestrogen, ICI 182 780, revealed cross-resistance. Sequence analysis of the hormone-binding domain of the OR of both lines showed no differences, suggesting that either mutations in other regions of the OR are involved in the TAM-resistance phenotype or that mechanisms outside of this protein induced this phenotype. Oestrogen and anti-oestrogen regulate pS2 and cathepsin D expression in 3366 tumours as in the human breast cancer cell line MCF-7. The resistant 3366/TAM tumours have lost this regulation. The established breast cancer xenografts 3366 and 3366/TAM offer the possibility of investigating mechanisms of anti-oestrogen resistance in an in vivo situation. They can be used to test novel approaches to prevent, or to overcome, this resistance in a clinically related manner. © 2000 Cancer Research Campaign

Similar content being viewed by others

Cystathionine-γ-lyase contributes to tamoxifen resistance, and the compound I194496 alleviates this effect by inhibiting the PPARγ/ACSL1/STAT3 signalling pathway in oestrogen receptor-positive breast cancer

Article Open access 03 October 2024

Tafazzin mediates tamoxifen resistance by regulating cellular phospholipid composition in ER-positive breast cancer

Article 07 November 2023

MiR-363-3p induces tamoxifen resistance in breast cancer cells through PTEN modulation

Article Open access 30 December 2024

Article PDF

Change history

  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

References

  • Augereau P, Garcia M, Mattei MG, Cavailles V, Depadova F, Derocq D, Capony F, Ferrara P and Rochefort H (1988) Cloning and sequencing of the 52K cathepsin D complementary deoxyribonucleic acid of MCF-7 breast cancer cells and mapping on chromosome 11. Mol Endocrinol 2: 186–192

    Article  CAS  Google Scholar 

  • Barkhem T, Carlsson B, Nilsson Y, Enmark E, Gustafsson JA and Nilsson S (1998) Differential response of oestrogen receptor α and oestrogen receptor β to partial oestrogen agonists/antagonists. Mol Pharmacol 54: 105–112

    Article  CAS  Google Scholar 

  • Brzozowski AM, Pike ACW, Dauter Z, Hubbart RE, Bonn T, Engström O, Öhman L, Green GL, Gustafsson JA and Carlquist M (1997) Molecular basis of agonism and antagonism in the oestrogen receptor. Nature 389: 753–758

    Article  CAS  Google Scholar 

  • Clarke R (1996) Human breast cancer cell line xenografts as models of breast cancer – The immunobiologies of recipient mice and the characteristics of several tumorigenic cell lines. Breast Cancer Res Treat 39: 69–86

    Article  CAS  Google Scholar 

  • Denton RR, Koszewski NJ and Notides AC (1992) Oestrogen receptor phosphorylation. Hormonal dependence and consequence on specific DNA binding. J Biol Chem 267: 7263–7268

    CAS  Google Scholar 

  • Early Breast Cancer Trial Collaborative Group (1992) Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy: 133 randomized trials involving 31 000 recurrences and 24 000 deaths among 75 000 women. Lancet 339: 1–15, 71–85

  • Foekens JA, Portengen H, Look MP, van Putten WLJ, Thirion B, Bontenbal M and Klijn JGM (1994) Relationship of PS2 with response to tamoxifen therapy in patients with recurrent breast cancer. Br J Cancer 70: 1217–1223

    Article  CAS  Google Scholar 

  • Gottardis MM and Jordan VC (1988) Development of tamoxifen-stimulated growth of MCF-7 tumors in athymic mice after long-term anti-oestrogen administration. Cancer Res 48: 5183–5187

    CAS  Google Scholar 

  • Green S, Walter P, Kumar V, Krust A, Bornert JM, Argos P and Chambon P (1986) Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A. Nature 320: 134–139

    Article  CAS  Google Scholar 

  • Jensen BL, Skouv J, Lundholt BK and Lykkesfeldt AE (1999) Differential regulation of specific genes in MCF-7 and the ICI 182780-resistant cell line MCF-7/182R-6. Br J Cancer 79: 386–392

    Article  CAS  Google Scholar 

  • Johnston SRD, Saccani-Jotti G, Smith IE, Salter J, Newby J, Coppen M, Ebbs SR and Dowsett M (1995) Changes in oestrogen receptor, progesterone receptor, and pS2 expression in tamoxifen-resistant human breast cancer. Cancer Res 55: 3331–3338

    CAS  Google Scholar 

  • Karnik PS, Julkarni S, Liu XP, Budd T and Bukowski RM (1994) Oestrogen receptor mutations in tamoxifen-resistant breast cancer. Cancer Res 54: 349–353

    CAS  Google Scholar 

  • Katzenellenbogen BS, Montano MM, Ekena K, Herman ME and McInerney EM (1997) Anti-oestrogens: mechanisms of action and resistance in breast cancer. Breast Cancer Res Treat 44: 23–38

    Article  CAS  Google Scholar 

  • Landel CC, Kushner PJ and Greene GL (1994) The interaction of human oestrogen receptor with DNA is modulated by receptor-associated proteins. Mol Endocrinol 8: 1407–1419

    CAS  Google Scholar 

  • Laborda J (1991) 36B4 cDNA used as an estradiol-independent mRNA control is the cDNA for human acidic ribosomal phosphoprotein PO. Nucleic Acids Res 19: 3998

    Article  CAS  Google Scholar 

  • Larsen SS, Madsen MW, Jensen BL and Lykkesfeldt AE (1997) Resistance of human breast-cancer cells to the pure steroidal anti-estrogen ICI 182,780 is not associated with a general loss of estrogen-receptor expression or lack of estrogen responsiveness. Int J Cancer 72: 1129–1136

    Article  CAS  Google Scholar 

  • Lavinsky RM, Jepsen K, Heinzel T, Torchia J, Mullen TM, Schiff R, Del Rio AL, Ricote M, Ngo S, Gemsch J, Hilsenbeck SG, Osborne CK, Glass CK, Rosenfeld MG and Rose DW (1998) Diverse signaling pathways modulate nuclear receptor recruitment of N-CoR and SMRT complexes. Proc Natl Acad Sci USA 95: 2920–2925

    Article  CAS  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL and Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193: 265–275

    CAS  Google Scholar 

  • Lykkesfeldt AE, Madsen MW and Briand P (1994) Altered expression of estrogen-regulated genes in a tamoxifen-resistant and ICI 164,384 and ICI 182,780 sensitive human breast cancer cell line, MCF-7/TAMR-1. Cancer Res 54: 1587–1595

    CAS  Google Scholar 

  • Lykkesfeldt AE (1996) Mechanisms of tamoxifen resistance in the treatment of advanced breast cancer. Acta Oncol 5: 9–14

    Article  Google Scholar 

  • Lykkesfeldt AE (1997). Growth regulation of human breast cancer cells by oestrogens and anti-oestrogens,

  • Maalouf GJ, Xu W, Smith TF and Mohr SC (1998) Homology model for the ligand-binding domain of the human estrogen receptor. J Biomol Struct Dyn 15: 841–851

    Article  CAS  Google Scholar 

  • Madsen MW, Lykkesfeldt AE, Laursen I, Nielsen KV and Briand P (1992) Altered gene expression of c-myc, epidermal growth factor receptor, transforming growth factor-alpha, and c-erb-B2 in an immortalized human breast epithelial cell line, HMT-3522, is associated with decreased growth factor requirements. Cancer Res 52: 1210–1217

    CAS  Google Scholar 

  • Madsen MW, Reiter BE, Larson SS, Briand P and Lykkesfeldt AE (1997) Estrogen receptor messenger RNA splice variants are not involved in antiestrogen resistance in sublines of MCF-7 human breast cancer cells. Cancer Res 57: 585–589

    CAS  Google Scholar 

  • Mahfoudi A, Roulet E, Dauvois S, Parker MG and Wahli W (1995) Specific mutations in the estrogen receptor change the properties of antiestrogens to full agonists. Proc Natl Acad Sci USA 92: 4206–4210

    Article  CAS  Google Scholar 

  • Martin MB, Saceda M, Garcia-Morales P and Gottardis MM (1994) Regulation of estrogen receptor expression. Breast Cancer Res Treat 31: 183–189

    Article  CAS  Google Scholar 

  • Masiakowski P, Breathnach R, Bloch J, Gannon F, Krust A and Chambon P (1982) Cloning of cDNA sequences of hormone-regulated genes from the MCF-7 human breast cancer cell line. Nucleic Acids Res 10: 7895–7903

    Article  CAS  Google Scholar 

  • Montano MM, Muller V, Trobaugh A and Katzenellenbogen BS (1995) The carboxy-terminal F domain of the human estrogen receptor: role in the transcriptional activity of the receptor and the effectiveness of antiestrogens as estrogen antagonists. Mol Endocrinol 9: 814–825

    CAS  Google Scholar 

  • Montella M, Biondi E, deMarco M, Cerra M, Cecco L, Botti G, Bonelli P and Tuccillo F (1996) Breast cancer estrogen and progesterone receptors: a multivariate analysis of associations with clinical and histologic characteristics in a series of 2933 consecutive cases. International Journal of Oncology 9: 977–982

    CAS  Google Scholar 

  • Murphy CS, Langan-Fahey SM, McCague R and Jordan VC (1990) Structure–function relationship of hydroxylated metabolites of tamoxifen that control the proliferation of estrogen-responsive T47D breast cancer cells in vivo. Mol Pharmacol 38: 737–743

    CAS  Google Scholar 

  • Murphy LC, Wang M, Coutt A and Dotzlaw H (1996) Novel mutations in the estrogen receptor messenger RNA in human breast cancers. J Clin Endocrinol Metab 81: 1420–1427

    CAS  Google Scholar 

  • Naundorf H and Arnold W (1981) Breeding of nude mice under improved conditions. Zeitschrift fur Versuchstierkunde 23: 77–79

    CAS  Google Scholar 

  • Naundorf H, Fichtner I, Büttner B and Frege J (1992) Establishment and characterization of a new human oestradiol – and progesterone-receptor-positive mammary carcinoma serially transplantable in nude mice. J Cancer Res Clin Oncol 119: 35–40

    Article  CAS  Google Scholar 

  • Noguchi S, Motomura K, Inaji H, Imaoka S and Koyama H (1993) Up-regulation of estrogen receptor by tamoxifen in human breast cancer. Cancer 71: 1266–1272

    Article  CAS  Google Scholar 

  • Osborne CK, Coronado EB and Robinson JP (1987) Human breast cancer in the athymic nude mouse: cytostatic effects of long-term antiestrogen therapy. European Journal of Cancer and Clinical Oncology 23: 1189–1196

    Article  CAS  Google Scholar 

  • Osborne CK and Fuqua SAW (1994) Mechanisms of tamoxifen resistance. Breast Cancer Res Treat 32: 49–55

    Article  CAS  Google Scholar 

  • Paech K, Webb P, Kuiper GGJM, Nilsson S, Gustafsson JA, Kushner PJ and Scanlan TS (1997) Differential ligand activation of oestrogen receptors ERα and ERβ at AP1 sites. Science 277: 1508–1510

    Article  CAS  Google Scholar 

  • Pink JJ and Jordan VC (1996) Models of estrogen receptor regulation by oestrogens and antiestrogens in breast cancer cell lines. Cancer Res 56: 2321–2330

    CAS  Google Scholar 

  • Rio MC, Bellocq JP, Gairard B, Rasmussen UB, Krust A, Koehl C, Calderoli H, Schiff V, Renaud R and Chambon P (1987) Specific expression of the pS2 gene in subclasses of breast cancers in comparison with expression of the estrogen and progesterone receptors and the oncogene ERBB2. Proc Natl Acad Sci USA 84: 9243–9247

    Article  CAS  Google Scholar 

  • Thompson EW, Brünner N, Torri J, Johnson MD, Boulay V, Wright A, Lippman ME, Steeg PS and Clarke R (1993) The invasive and metastatic properties of hormone-independent but hormone-responsive variants of MCF-7 human breast cancer cells. Clin Exp Metastasis 11: 15–26

    Article  CAS  Google Scholar 

  • Tonetti DA and Jordan VC (1995) Possible mechanisms in the emergence of tamoxifen-resistant breast cancer. Anticancer Drugs 6: 498–507

    Article  CAS  Google Scholar 

  • Tonetti DA and Jordan VC (1997) The role of estrogen receptor mutations in tamoxifen-stimulated breast cancer. J Steroid Biochem Mol Biol 62: 119–128

    Article  CAS  Google Scholar 

  • van Agthoven T, van Agthoven TLA, Dekker A, van der Spek PJ, Vreede L and Dorssers LCJ (1998) Identification of BCAR3 by a random search for genes involved in antiestrogen resistance of human breast cancer cells. EMBO J 17: 2799–2808

    Article  CAS  Google Scholar 

  • Westley B and Rochefort H (1980) A secreted glycoprotein induced by estrogen in human breast cancer cell lines. Cell 20: 353–362

    Article  CAS  Google Scholar 

  • Westley B, May FEB, Brown AMC, Krust A, Chambon P, Lippman ME and Rochefort H (1984) Effects of antiestrogens on the estrogen-regulated pS2 RNA and the 52- and 160-kilodalton proteins in MCF-7 cells and two tamoxifen resistant sublines. J Biol Chem 259: 10030–10035

    CAS  Google Scholar 

  • Wolf DM and Jordan VC (1994) Characterization of tamoxifen stimulated MCF-7 tumor variants grown in athymic mice. Breast Cancer Res Treat 31: 117–127

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Strasse 10, Berlin, 13092, Germany

    H Naundorf, M Becker, B Elbe, C Neumann, B Büttner & I Fichtner

  2. Institute of Cancer Biology, Danish Cancer Society, Strandboulevarden 49, Copenhagen, DK-2100, Denmark

    A E Lykkesfeldt

Authors
  1. H Naundorf
    View author publications

    Search author on:PubMed Google Scholar

  2. M Becker
    View author publications

    Search author on:PubMed Google Scholar

  3. A E Lykkesfeldt
    View author publications

    Search author on:PubMed Google Scholar

  4. B Elbe
    View author publications

    Search author on:PubMed Google Scholar

  5. C Neumann
    View author publications

    Search author on:PubMed Google Scholar

  6. B Büttner
    View author publications

    Search author on:PubMed Google Scholar

  7. I Fichtner
    View author publications

    Search author on:PubMed Google Scholar

Rights and permissions

From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

Reprints and permissions

About this article

Cite this article

Naundorf, H., Becker, M., Lykkesfeldt, A. et al. Development and characterization of a tamoxifen-resistant breast carcinoma xenograft. Br J Cancer 82, 1844–1850 (2000). https://doi.org/10.1054/bjoc.2000.1156

Download citation

  • Received: 09 September 1999

  • Revised: 13 January 2000

  • Accepted: 18 January 2000

  • Published: 04 May 2000

  • Issue date: 01 June 2000

  • DOI: https://doi.org/10.1054/bjoc.2000.1156

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • tamoxifen resistance
  • breast cancer
  • xenograft
  • oestrogen receptor
  • cathepsin D gene
  • pS2 gene

This article is cited by

  • Steroid Hormone Receptor Positive Breast Cancer Patient-Derived Xenografts

    • Shawna B. Matthews
    • Carol A. Sartorius

    Hormones and Cancer (2017)

  • Systematic drug screening reveals specific vulnerabilities and co-resistance patterns in endocrine-resistant breast cancer

    • Sara Kangaspeska
    • Susanne Hultsch
    • Olli Kallioniemi

    BMC Cancer (2016)

  • Characterisation of breast cancer cell lines and establishment of a novel isogenic subclone to study migration, invasion and tumourigenicity

    • Linda Hughes
    • Catherine Malone
    • Susan McDonnell

    Clinical & Experimental Metastasis (2008)

  • The mTOR pathway inhibitor RAD001 (everolimus) is highly efficacious in tamoxifen-sensitive and -resistant breast cancer xenografts

    • Diana Behrens
    • Anne E. Lykkesfeldt
    • Iduna Fichtner

    Targeted Oncology (2007)

  • Tamoxifen-resistant breast carcinoma xenograft

    • Valerie Speirs

    Breast Cancer Research (2000)

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Current issue
  • Collections
  • Follow us on Twitter
  • Sign up for alerts
  • RSS feed

About the journal

  • Journal Information
  • Open access publishing
  • About the Editors
  • Contact
  • Special Issues
  • For Advertisers
  • Subscribe

Publish with us

  • For Authors & Referees
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

British Journal of Cancer (Br J Cancer)

ISSN 1532-1827 (online)

ISSN 0007-0920 (print)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited