Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Retinoic acid receptor and retinoid X receptor in ductal carcinoma in situ and intraductal proliferative lesions of the human breast.

Japanese journal of cancer research : Gann - 1 Nov 2000

Ariga N, Moriya T, Suzuki T, Kimura M, Ohuchi N, Sasano H

Abstract excerpt

Retinoic acid (RAR) and retinoid X receptors (RXR) are essential in the transcriptional actions of retinoids. To date, RAR and RXR have not been examined in precancerous lesions and / or ductal carcinoma in situ (DCIS) in human breast. Therefore, we examined RAR and RXR subtypes in DCIS (58 cases), atypical ductal hyperplasia (ADH) (32 cases), and proliferative disease without atypia (PDWA) (32 cases) to study...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Breast
Share to Carcinoma, Ductal, Breast

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Carcinoma in Situ

Share to Ki-67 Antigen

Share to Receptors, Progesterone

Share to Receptors, Retinoic Acid

Share to Retinoic Acid Receptor alpha

Share to Retinoid X Receptors

Source

Open in PubMed Open full text

Identifiers

PMID: 11092983
DOI: 10.1111/j.1349-7006.2000.tb00901.x
PMCID: PMC5926283

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Retinoic acid receptor and retinoid X receptor in ductal carcinoma in situ and intraductal proliferative lesions of the human breast.PMID 11092983Read ↗

Alteration in protein expression in estrogen receptor alpha-negative human breast cancer tissues indicates a malignant and metastatic phenotype.Semantic proximity Read ↗

Promoter Methylation of the Retinoic Acid Receptor Beta2 (RARβ2) Is Associated with Increased Risk of Breast Cancer: A PRISMA Compliant Meta-Analysis.Semantic proximity Read ↗

Comprehensive expression analysis of retinoic acid receptors and retinoid X receptors in non-small cell lung cancer: implications for tumor development and prognosisSemantic proximity Read ↗

Research resource: transcriptome profiling of genes regulated by RXR and its permissive and nonpermissive partners in differentiating monocyte-derived dendritic cells.Semantic proximity Read ↗

Activation of aromatase expression by retinoic acid receptor-related orphan receptor (ROR) alpha in breast cancer cells: identification of a novel ROR response element.Semantic proximity Read ↗

A repressive epigenetic domino effect confers susceptibility to breast epithelial cell transformation: implications for predicting breast cancer risk.Semantic proximity Read ↗

The Influence of 13- cis Retinoic Acid on Human Meibomian Gland Epithelial CellsSemantic proximity Read ↗

The rexinoid, bexarotene, prevents the development of premalignant lesions in MMTV-erbB2 miceSemantic proximity Read ↗

Methylation and Silencing of the Retinoic Acid Receptor- 2 Gene in Breast CancerSemantic proximity Read ↗

Retinoic Acid and Retinoid X Receptors Are Differentially Expressed in Thyroid Cancer and Thyroid Carcinoma Cell Lines and Predict Response to Treatment with RetinoidsSemantic proximity Read ↗

Expression of miR-21 and its targets (PTEN, PDCD4, TM1) in flat epithelial atypia of the breast in relation to ductal carcinoma in situ and invasive carcinomaSemantic proximity Read ↗

Estrogen induces retinoid receptor expression in mouse cervical epithelia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.