Literature DB >> 17125601

Interstitial cells of Cajal (ICC) and gastrointestinal stromal tumor (GIST): facts, speculations, and myths.

K W Min1, M Leabu.   

Abstract

Interstitial cells of Cajal (ICC) is a peculiar cell network composed of cells having processes described by the eminent Spanish neuroanatomist of the 19th century, S. Ramon y Cajal. ICC became a fascinating subject to many investigators and it is estimated that there are over 100 publications yearly on the subject related to ICC, in the last three years. Now it is widely accepted that ICC are pace maker cells of the gut and probable progenitor cells of gastrointestinal stromal tumors (GIST). Lately, interstitial Cajal-like cells (ICLC) are being found in various organs and their physiological role is still to be defined. We have reviewed the literature trying to evaluate the validity of the current concept and found that there are a few salient points to be considered. 1) There has been some important departure in defining the identity of ICC from the original criteria of Cajal. In particular, ICC with myoid feafures in intestinal smooth muscle layers (ICC-DPM) do not seem to fit to the original description of interstitial cell network by Cajal. We have also pointed out that the current reports assigning a pace maker role to ICC vastly depend on the scientific data on "ICC with myoid features", not on "fibroblast-like ICC", which are more abundant and easier to identify. 2) There seem to be an overwhelming amount of data proving the relationship between ICC and GIST. Both are known to express c-Kit and the ultrastructural characteristics seen in GIST roughly parallel those of ICC including minimal myoid differentiation seen in the majority of GIST, supporting the current concept that GIST are ICC tumors. 3) According to the original description of Cajal, ICC was not limited to the gut, suggesting an existence of ICC in other organs. The list of organs reported to contain ICC (currently identified by immunohistochemistry and electron microscopy) is ever growing and further studies are needed to define their identity and pathophysiologic role. 4). Recent data concerning gut development suggest that both c-Kit expressing ICC (fibroblasts-like as well as muscle-like) and gut muscle cells derive from the common progenitor cells of the embryonic gut unifying the histogenetic concept of all GIST with heterogeneous cytomorphologic features. In this review we attempted to incorporate recent information on interstitial Cajal-like cells (ICLC) found in other organs to broaden our understanding of ICC in general in terms of their ultrastructure, physiology, and neoplasia.

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Year:  2006        PMID: 17125601      PMCID: PMC3933091          DOI: 10.1111/j.1582-4934.2006.tb00541.x

Source DB:  PubMed          Journal:  J Cell Mol Med        ISSN: 1582-1838            Impact factor:   5.310


  102 in total

1.  Developmental origin and Kit-dependent development of the interstitial cells of cajal in the mammalian small intestine.

Authors:  M Klüppel; J D Huizinga; J Malysz; A Bernstein
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2.  Gastrointestinal autonomic nerve tumor: immunohistochemical and molecular identity with gastrointestinal stromal tumor.

Authors:  J R Lee; V Joshi; J W Griffin ; J Lasota; M Miettinen
Journal:  Am J Surg Pathol       Date:  2001-08       Impact factor: 6.394

3.  Fine structure of the myenteric plexus in the guinea-pig ileum.

Authors:  G Gabella
Journal:  J Anat       Date:  1972-01       Impact factor: 2.610

4.  Light- and electron microscopical studies of interstitial cells of Cajal and muscle cells at the submucosal border of human colon.

Authors:  J J Rumessen; S Peters; L Thuneberg
Journal:  Lab Invest       Date:  1993-04       Impact factor: 5.662

5.  Ultrastructure of interstitial cells of Cajal in circular muscle of human small intestine.

Authors:  J J Rumessen; H B Mikkelsen; K Qvortrup; L Thuneberg
Journal:  Gastroenterology       Date:  1993-02       Impact factor: 22.682

6.  Subclassification of gastrointestinal stromal tumors based on evaluation by electron microscopy and immunohistochemistry.

Authors:  R A Erlandson; D S Klimstra; J M Woodruff
Journal:  Ultrastruct Pathol       Date:  1996 Jul-Aug       Impact factor: 1.094

7.  Stromal tumor of the pancreas with expression of c-kit protein: report of a case.

Authors:  Kazuhiro Yamaura; Kunitaka Kato; Masahisa Miyazawa; Yoshiaki Haba; Akira Muramatsu; Kazuyuki Miyata; Naohiko Koide
Journal:  J Gastroenterol Hepatol       Date:  2004-04       Impact factor: 4.029

8.  Small intestinal stromal tumors with skeinoid fibers in neurofibromatosis: report of four cases with ultrastructural study of skeinoid fibers from paraffin blocks.

Authors:  K W Min; A J Balaton
Journal:  Ultrastruct Pathol       Date:  1993 May-Aug       Impact factor: 1.094

9.  Interstitial cells of Cajal generate a rhythmic pacemaker current.

Authors:  L Thomsen; T L Robinson; J C Lee; L A Farraway; M J Hughes; D W Andrews; J D Huizinga
Journal:  Nat Med       Date:  1998-07       Impact factor: 53.440

10.  Origin of the c-kit-positive interstitial cells in the avian bowel.

Authors:  L Lecoin; G Gabella; N Le Douarin
Journal:  Development       Date:  1996-03       Impact factor: 6.868

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  26 in total

1.  Interstitial Cajal-like cells of human Fallopian tube express estrogen and progesterone receptors.

Authors:  Sanda Maria Cretoiu; D Cretoiu; Laura Suciu; L M Popescu
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2.  Ultra-structural identification of interstitial cells of Cajal in the zebrafish Danio rerio.

Authors:  Evan R Ball; Miho M Matsuda; Louis Dye; Victoria Hoffmann; Patricia M Zerfas; Eva Szarek; Adam Rich; Ajay B Chitnis; Constantine A Stratakis
Journal:  Cell Tissue Res       Date:  2012-05-25       Impact factor: 5.249

3.  Plexiform myxoid gastrointestinal stromal tumor: a potential diagnostic pitfall in pathological findings.

Authors:  Bo Li; Qing-Fu Zhang; Yu-Nan Han; Ling Ouyang
Journal:  Int J Clin Exp Pathol       Date:  2015-10-01

4.  Successful imatinib therapy for neuroendocrine carcinoma with activating Kit mutation: a case study.

Authors:  James Perkins; Patrick Boland; Steven J Cohen; Anthony J Olszanski; Yan Zhou; Paul Engstrom; Igor Astsaturov
Journal:  J Natl Compr Canc Netw       Date:  2014-06       Impact factor: 11.908

Review 5.  Rare gastrointestinal stromal tumors (GIST): omentum and retroperitoneum.

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Journal:  Transl Gastroenterol Hepatol       Date:  2017-12-19

6.  Diagnostic challenges of motility disorders: optimal detection of CD117+ interstitial cells of Cajal.

Authors:  Megan M Garrity; Simon J Gibbons; Thomas C Smyrk; Jean Marie Vanderwinden; Pedro Julian Gomez-Pinilla; Anoop Nehra; Matthew Borg; Gianrico Farrugia
Journal:  Histopathology       Date:  2009-02       Impact factor: 5.087

7.  Primary gastrointestinal stromal tumor of the liver: A case report and review of the literature.

Authors:  Xiaobin Cheng; Dong Chen; Wenbin Chen; Qinsong Sheng
Journal:  Oncol Lett       Date:  2016-08-10       Impact factor: 2.967

8.  Secondary mutations of c-KIT contribute to acquired resistance to imatinib and decrease efficacy of sunitinib in Chinese patients with gastrointestinal stromal tumors.

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Journal:  Med Oncol       Date:  2013-03-02       Impact factor: 3.064

Review 9.  Targeting of cancer stem/progenitor cells plus stem cell-based therapies: the ultimate hope for treating and curing aggressive and recurrent cancers.

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Journal:  Panminerva Med       Date:  2008-03       Impact factor: 5.197

10.  Primary extragastrointestinal stromal tumor of the transverse mesocolon without c-kit mutations but with PDGFRA mutations.

Authors:  Tadashi Terada
Journal:  Med Oncol       Date:  2008-09-08       Impact factor: 3.064

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