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PEComas: the past, the present and the future.

Abstract
The perivascular epithelioid cell (PEC) is a cell type constantly present in a group of tumors called PEComas. PEC expresses myogenic and melanocytic markers, such as HMB45 and actin. Recently, recurrent chromosomal alterations have been demonstrated in PEC. At present, PEComa is a widely accepted entity. In the past 10 years, the use of this term has allowed to report and describe numerous cases permitting to start highlighting the biology of this group of lesions. PEComas are related to the genetic alterations of tuberous sclerosis complex (TSC), an autosomal dominant genetic disease due to losses of TSC1 (9q34) or TSC2 (16p13.3) genes which seem to have a role in the regulation of the Rheb/mTOR/p70S6K pathway. There are some open questions about PEComas regarding its histogenesis, the definition of epithelioid angiomyolipoma and the identification of the histological criteria of malignancy. An innovative therapeutic trial using rapamycin is under way for tumors occurring in TSC such as renal angiomyolipoma and lymphangioleiomyomatosis. Its success could provide the rationale for the use of the same drug in other lesions composed of PECs, especially in the malignant ones.
AuthorsGuido Martignoni, Maurizio Pea, Daniela Reghellin, Giuseppe Zamboni, Franco Bonetti
JournalVirchows Archiv : an international journal of pathology (Virchows Arch) Vol. 452 Issue 2 Pg. 119-32 (Feb 2008) ISSN: 0945-6317 [Print] Germany
PMID18080139 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Biomarkers, Tumor
  • Neoplasm Proteins
  • TSC1 protein, human
  • TSC2 protein, human
  • Tuberous Sclerosis Complex 1 Protein
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins
Topics
  • Angiomyolipoma (genetics, metabolism, pathology)
  • Biomarkers, Tumor (metabolism)
  • Chromosome Aberrations
  • Epithelioid Cells (metabolism, pathology)
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Neoplasm Proteins (metabolism)
  • Tuberous Sclerosis (genetics, metabolism, pathology)
  • Tuberous Sclerosis Complex 1 Protein
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins (genetics, metabolism)

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