<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(6)</volume><submitter>Borley AC</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Anti-oestrogens have been the mainstay of therapy in patients with oestrogen-receptor (ER) positive breast cancer and have provided significant improvements in survival. However, their benefits are limited by tumour recurrence in a significant proportion of initially drug-responsive breast cancer patients because of acquired anti-oestrogen resistance. Relapse on such therapies clinically presents as local and/or regional recurrences, frequently with distant metastases, and the prognosis for these patients is poor. The selective ER modulator, tamoxifen, classically exerts gene inhibitory effects during the drug-responsive phase in ER-positive breast cancer cells. Paradoxically, this drug is also able to induce the expression of genes, which in the appropriate cell conte</pubmed_abstract><journal>Breast cancer research : BCR</journal><pagination>R103</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2656899</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Anti-oestrogens but not oestrogen deprivation promote cellular invasion in intercellular adhesion-deficient breast cancer cells.</pubmed_title><pmcid>PMC2656899</pmcid><pubmed_authors>Barrett-Lee P</pubmed_authors><pubmed_authors>Nicholson RI</pubmed_authors><pubmed_authors>Smith C</pubmed_authors><pubmed_authors>Gee J</pubmed_authors><pubmed_authors>Borley AC</pubmed_authors><pubmed_authors>Shaw V</pubmed_authors><pubmed_authors>Hiscox S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anti-oestrogens but not oestrogen deprivation promote cellular invasion in intercellular adhesion-deficient breast cancer cells.</name><description>&lt;h4>Introduction&lt;/h4>Anti-oestrogens have been the mainstay of therapy in patients with oestrogen-receptor (ER) positive breast cancer and have provided significant improvements in survival. However, their benefits are limited by tumour recurrence in a significant proportion of initially drug-responsive breast cancer patients because of acquired anti-oestrogen resistance. Relapse on such therapies clinically presents as local and/or regional recurrences, frequently with distant metastases, and the prognosis for these patients is poor. The selective ER modulator, tamoxifen, classically exerts gene inhibitory effects during the drug-responsive phase in ER-positive breast cancer cells. Paradoxically, this drug is also able to induce the expression of genes, which in the appropriate cell conte</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008</publication><modification>2025-04-04T19:12:53.586Z</modification><creation>2019-03-27T00:21:17Z</creation></dates><accession>S-EPMC2656899</accession><cross_references><pubmed>19055788</pubmed><doi>10.1186/bcr2206</doi></cross_references></HashMap>