Literature DB >> 2479695

Unusual patterns of keratin expression in the overlying epidermis of patients with dermatofibromas: biochemical alterations in the epidermis as a consequence of dermal tumors.

A Stoler1, M Duvic, E Fuchs.   

Abstract

Dermatofibromas are frequently associated with acanthosis of the overlying epidermis. Using monospecific antisera and cRNA probes, we have examined the pattern of expression of keratin and keratin mRNA in the affected epidermis of patients with these dermal tumors. Our studies reveal several abnormalities in keratin expression within the thickened areas of overlying epidermis. In two of 15 patients, we detected K6 and K16, keratins which are frequently associated with epidermal diseases of hyperproliferation but are not present in normal epidermis. In both cases, K6 and K16 were found in suprabasal layers, similar to that seen for psoriasis and squamous cell carcinomas. Expression of K6 and K16 in skin samples from patients with dermatofibromas seemed to be dependent upon how near was the tumor to the overlying epidermis, and possibly upon the degree of cellularity within the tumor mass. A second aberration in keratin expression, and one which did not appear to be linked to K6/K16 expression, was the altered expression of the basal epidermal keratin K14. Expression of this keratin and its mRNA was variable, often extending into multiple suprabasal layers and including both basal-like and squamous-like cells. In contrast to the expression of K6/K16, aberrant expression of K14 was a relatively frequent event, occurring in greater than 70% of the dermatofibroma skin samples examined. These observations provide the first biochemical evidence in support of previous morphologic studies, indicating that alterations in epidermal differentiation can occur as a consequence of dermal skin tumors.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2479695     DOI: 10.1111/1523-1747.ep12284397

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  6 in total

1.  E-cadherin controls adherens junctions in the epidermis and the renewal of hair follicles.

Authors:  Peter Young; Oreda Boussadia; Hartmut Halfter; Richard Grose; Philipp Berger; Dino P Leone; Horst Robenek; Patrick Charnay; Rolf Kemler; Ueli Suter
Journal:  EMBO J       Date:  2003-11-03       Impact factor: 11.598

2.  Increased telomere fragility and fusions resulting from TRF1 deficiency lead to degenerative pathologies and increased cancer in mice.

Authors:  Paula Martínez; Maria Thanasoula; Purificación Muñoz; Chunyan Liao; Agueda Tejera; Carolyn McNees; Juana M Flores; Oscar Fernández-Capetillo; Madalena Tarsounas; Maria A Blasco
Journal:  Genes Dev       Date:  2009-08-13       Impact factor: 11.361

3.  Protein and mRNA expression of simple epithelial keratins in normal, dysplastic, and malignant oral epithelia.

Authors:  L Su; P R Morgan; E B Lane
Journal:  Am J Pathol       Date:  1994-12       Impact factor: 4.307

4.  TPP1 is required for TERT recruitment, telomere elongation during nuclear reprogramming, and normal skin development in mice.

Authors:  Agueda M Tejera; Martina Stagno d'Alcontres; Maria Thanasoula; Rosa M Marion; Paula Martinez; Chunyan Liao; Juana M Flores; Madalena Tarsounas; Maria A Blasco
Journal:  Dev Cell       Date:  2010-05-18       Impact factor: 13.417

5.  Transformation of human urothelial cells (UROtsa) by as and cd induces the expression of keratin 6a.

Authors:  Seema Somji; Chandra S Bathula; Xu Dong Zhou; Mary Ann Sens; Donald A Sens; Scott H Garrett
Journal:  Environ Health Perspect       Date:  2008-04       Impact factor: 9.031

6.  Non‑invasive proteome‑wide quantification of skin barrier‑related proteins using label‑free LC‑MS/MS analysis.

Authors:  Mengting Liu; Jing Zhang; Yaochi Wang; Cong Xin; Jie Ma; Shuangjun Xu; Xiaomeng Wang; Jinping Gao; Xuejun Zhang; Sen Yang
Journal:  Mol Med Rep       Date:  2020-03-11       Impact factor: 2.952

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.