Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors

Nadine Darwiche, Giulia Celli, Tamar Tennenbaum, Adam Bleier Glick, Stuart H. Yuspa, Luigi M. De Luca

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

Retinoids are powerful regulators of epidermal cell growth and differentiation and are widely used in the prevention and treatment of skin disorders and cancers in humans. Since many of the effects of retinoids on cell growth and differentiation are mediated by nuclear retinoid receptors (RARs and RXRs), we were interested in determining RAR and RXR gene expression during mouse skin tumor progression. The two-stage system of mouse skin carcinogenesis was used to generate papillomas and carcinomas, and the different stages of malignant progression (papillomas, differentiated squamous cell carcinomas, undifferentiated squamous cell carcinomas, and spindle cell carcinomas) were characterized in each tumor by specific keratin expression prior to receptor characterization. Using in situ hybridization analysis, we show that the two major RAR isoforms (α1 and γ1), which account for most of RARs in the skin, were expressed in both the basal and suprabasal layers in mouse epidermis. In contrast, RXRa transcripts were compartmentalized to the basal cell layers and concentrated in hair follicles. During skin tumor progression, RAR (α1 and γ1) transcripts were down-modulated in malignant tumor cells, whereas RXR (α and β) transcript expression was expanded in papillomas and carcinomas as the number of undifferentiated cells also increased. RXR γ was not detected in the skin or at any stage during skin tumor progression. Spindle cell tumors lacked markers of the keratinocyte phenotype and lost RAR expression, yet retained expression of RXRα and β. The increased abundance of transcripts for RXRs and decreased presence of RARs in skin tumor progression may favor other nuclear signal transduction pathways requiring RXR for heterodimer formation and contribute to phenotypic progression of cancer cells.

Original languageEnglish (US)
Pages (from-to)2774-2782
Number of pages9
JournalCancer Research
Volume55
Issue number13
StatePublished - Jul 1 1995

Fingerprint

Retinoid X Receptors
Tretinoin
Skin
Retinoids
Papilloma
Neoplasms
Carcinoma
Cell Differentiation
Squamous Cell Carcinoma
Hair Follicle
Skin Neoplasms
Tumor Biomarkers
Cytoplasmic and Nuclear Receptors
Growth
Keratins
Keratinocytes
Epidermis
In Situ Hybridization
Signal Transduction
Protein Isoforms

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

Cite this

Darwiche, N., Celli, G., Tennenbaum, T., Glick, A. B., Yuspa, S. H., & De Luca, L. M. (1995). Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors. Cancer Research, 55(13), 2774-2782.
Darwiche, Nadine ; Celli, Giulia ; Tennenbaum, Tamar ; Glick, Adam Bleier ; Yuspa, Stuart H. ; De Luca, Luigi M. / Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors. In: Cancer Research. 1995 ; Vol. 55, No. 13. pp. 2774-2782.
@article{6b0979e60b7e45c5a1f1dfc7dcf75da3,
title = "Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors",
abstract = "Retinoids are powerful regulators of epidermal cell growth and differentiation and are widely used in the prevention and treatment of skin disorders and cancers in humans. Since many of the effects of retinoids on cell growth and differentiation are mediated by nuclear retinoid receptors (RARs and RXRs), we were interested in determining RAR and RXR gene expression during mouse skin tumor progression. The two-stage system of mouse skin carcinogenesis was used to generate papillomas and carcinomas, and the different stages of malignant progression (papillomas, differentiated squamous cell carcinomas, undifferentiated squamous cell carcinomas, and spindle cell carcinomas) were characterized in each tumor by specific keratin expression prior to receptor characterization. Using in situ hybridization analysis, we show that the two major RAR isoforms (α1 and γ1), which account for most of RARs in the skin, were expressed in both the basal and suprabasal layers in mouse epidermis. In contrast, RXRa transcripts were compartmentalized to the basal cell layers and concentrated in hair follicles. During skin tumor progression, RAR (α1 and γ1) transcripts were down-modulated in malignant tumor cells, whereas RXR (α and β) transcript expression was expanded in papillomas and carcinomas as the number of undifferentiated cells also increased. RXR γ was not detected in the skin or at any stage during skin tumor progression. Spindle cell tumors lacked markers of the keratinocyte phenotype and lost RAR expression, yet retained expression of RXRα and β. The increased abundance of transcripts for RXRs and decreased presence of RARs in skin tumor progression may favor other nuclear signal transduction pathways requiring RXR for heterodimer formation and contribute to phenotypic progression of cancer cells.",
author = "Nadine Darwiche and Giulia Celli and Tamar Tennenbaum and Glick, {Adam Bleier} and Yuspa, {Stuart H.} and {De Luca}, {Luigi M.}",
year = "1995",
month = "7",
day = "1",
language = "English (US)",
volume = "55",
pages = "2774--2782",
journal = "Cancer Research",
issn = "0008-5472",
number = "13",

}

Darwiche, N, Celli, G, Tennenbaum, T, Glick, AB, Yuspa, SH & De Luca, LM 1995, 'Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors', Cancer Research, vol. 55, no. 13, pp. 2774-2782.

Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors. / Darwiche, Nadine; Celli, Giulia; Tennenbaum, Tamar; Glick, Adam Bleier; Yuspa, Stuart H.; De Luca, Luigi M.

In: Cancer Research, Vol. 55, No. 13, 01.07.1995, p. 2774-2782.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors

AU - Darwiche, Nadine

AU - Celli, Giulia

AU - Tennenbaum, Tamar

AU - Glick, Adam Bleier

AU - Yuspa, Stuart H.

AU - De Luca, Luigi M.

PY - 1995/7/1

Y1 - 1995/7/1

N2 - Retinoids are powerful regulators of epidermal cell growth and differentiation and are widely used in the prevention and treatment of skin disorders and cancers in humans. Since many of the effects of retinoids on cell growth and differentiation are mediated by nuclear retinoid receptors (RARs and RXRs), we were interested in determining RAR and RXR gene expression during mouse skin tumor progression. The two-stage system of mouse skin carcinogenesis was used to generate papillomas and carcinomas, and the different stages of malignant progression (papillomas, differentiated squamous cell carcinomas, undifferentiated squamous cell carcinomas, and spindle cell carcinomas) were characterized in each tumor by specific keratin expression prior to receptor characterization. Using in situ hybridization analysis, we show that the two major RAR isoforms (α1 and γ1), which account for most of RARs in the skin, were expressed in both the basal and suprabasal layers in mouse epidermis. In contrast, RXRa transcripts were compartmentalized to the basal cell layers and concentrated in hair follicles. During skin tumor progression, RAR (α1 and γ1) transcripts were down-modulated in malignant tumor cells, whereas RXR (α and β) transcript expression was expanded in papillomas and carcinomas as the number of undifferentiated cells also increased. RXR γ was not detected in the skin or at any stage during skin tumor progression. Spindle cell tumors lacked markers of the keratinocyte phenotype and lost RAR expression, yet retained expression of RXRα and β. The increased abundance of transcripts for RXRs and decreased presence of RARs in skin tumor progression may favor other nuclear signal transduction pathways requiring RXR for heterodimer formation and contribute to phenotypic progression of cancer cells.

AB - Retinoids are powerful regulators of epidermal cell growth and differentiation and are widely used in the prevention and treatment of skin disorders and cancers in humans. Since many of the effects of retinoids on cell growth and differentiation are mediated by nuclear retinoid receptors (RARs and RXRs), we were interested in determining RAR and RXR gene expression during mouse skin tumor progression. The two-stage system of mouse skin carcinogenesis was used to generate papillomas and carcinomas, and the different stages of malignant progression (papillomas, differentiated squamous cell carcinomas, undifferentiated squamous cell carcinomas, and spindle cell carcinomas) were characterized in each tumor by specific keratin expression prior to receptor characterization. Using in situ hybridization analysis, we show that the two major RAR isoforms (α1 and γ1), which account for most of RARs in the skin, were expressed in both the basal and suprabasal layers in mouse epidermis. In contrast, RXRa transcripts were compartmentalized to the basal cell layers and concentrated in hair follicles. During skin tumor progression, RAR (α1 and γ1) transcripts were down-modulated in malignant tumor cells, whereas RXR (α and β) transcript expression was expanded in papillomas and carcinomas as the number of undifferentiated cells also increased. RXR γ was not detected in the skin or at any stage during skin tumor progression. Spindle cell tumors lacked markers of the keratinocyte phenotype and lost RAR expression, yet retained expression of RXRα and β. The increased abundance of transcripts for RXRs and decreased presence of RARs in skin tumor progression may favor other nuclear signal transduction pathways requiring RXR for heterodimer formation and contribute to phenotypic progression of cancer cells.

UR - http://www.scopus.com/inward/record.url?scp=0029058519&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0029058519&partnerID=8YFLogxK

M3 - Article

C2 - 7540949

AN - SCOPUS:0029058519

VL - 55

SP - 2774

EP - 2782

JO - Cancer Research

JF - Cancer Research

SN - 0008-5472

IS - 13

ER -

Darwiche N, Celli G, Tennenbaum T, Glick AB, Yuspa SH, De Luca LM. Mouse Skin Tumor Progression Results in Differential Expression of Retinoic Acid and Retinoid X Receptors. Cancer Research. 1995 Jul 1;55(13):2774-2782.