K-ras and p53 mutations in the pathogenesis of classical and goblet cell carcinoids of the appendix

Dharam M. Ramnani, Ignacio I. Wistuba, Carmen Behrens, Adi F. Gazdar, Leslie H. Sobin, Jorge Albores-Saavedra

Research output: Contribution to journalArticle

72 Citations (Scopus)

Abstract

BACKGROUND. Mutations in the K-ras oncogene and the p53 tumor suppressor gene are present in approximately 50% of colonic adenocarcinomas. Goblet cell carcinoids (GCCs) are uncommon neoplasms of the appendix that appear to be intermediate between carcinoid tumors and adenocarcinomas, both histologically and biologically. The current study was undertaken to examine the role of p53 and K-ras mutations in the pathogenesis of GCCs and typical carcinoids (TCs) of the appendix. METHODS. Archival materials from 22 GCCs and 18 TCs were analyzed. K-ras mutations in codons 12, 13, and 61 were studied by a polymerase chain reaction (PCR) based designed restriction fragment length polymorphism method using mismatched nested primers. Mutations in exons 5-8 of the p53 tumor suppressor gene were analyzed in 16 GCCs and 18 TCs by PCR and single-strand conformational polymorphism followed by direct sequencing. Immunostains for p53 and chromogranin were performed in all cases. RESULTS. K-ras mutations and nuclear accumulation of p53 by immunohistochemistry were not detected in any of the GCCs or TCs. p53 mutations were found in 4 of 16 GCCs (25%) and 8 of 18 TCs (44%). Immunoreactivity for chromogranin was seen in the vast majority of GCCs and TCs. CONCLUSIONS. p53 mutations appear to play a role in the pathogenesis of some GCCs and in approximately 50% of TCs of the appendix, whereas mutations in the K-ras oncogene do not appear to be important in the development of these tumors. The minimal cytologic atypia, low incidence of metastases, and lack of K-ras mutations in goblet cell appendiceal neoplasms suggest that they are variants of carcinoid tumors. Our findings lend support to the recommendation that the therapeutic guidelines applied to TCs of the appendix should be the same for GCCs.

Original languageEnglish (US)
Pages (from-to)14-21
Number of pages8
JournalCancer
Volume86
Issue number1
DOIs
StatePublished - Jul 1 1999

Fingerprint

Carcinoid Tumor
Mutation
Appendix
Chromogranins
ras Genes
Tumor Suppressor Genes
Appendiceal Neoplasms
Adenocarcinoma
Polymerase Chain Reaction
Goblet Cells

Keywords

  • Classical carcinoid of the appendix
  • Goblet cell carcinoid of the appendix
  • Immunohistochemistry
  • K-ras gene
  • p53 gene

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

K-ras and p53 mutations in the pathogenesis of classical and goblet cell carcinoids of the appendix. / Ramnani, Dharam M.; Wistuba, Ignacio I.; Behrens, Carmen; Gazdar, Adi F.; Sobin, Leslie H.; Albores-Saavedra, Jorge.

In: Cancer, Vol. 86, No. 1, 01.07.1999, p. 14-21.

Research output: Contribution to journalArticle

Ramnani, Dharam M. ; Wistuba, Ignacio I. ; Behrens, Carmen ; Gazdar, Adi F. ; Sobin, Leslie H. ; Albores-Saavedra, Jorge. / K-ras and p53 mutations in the pathogenesis of classical and goblet cell carcinoids of the appendix. In: Cancer. 1999 ; Vol. 86, No. 1. pp. 14-21.
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title = "K-ras and p53 mutations in the pathogenesis of classical and goblet cell carcinoids of the appendix",
abstract = "BACKGROUND. Mutations in the K-ras oncogene and the p53 tumor suppressor gene are present in approximately 50{\%} of colonic adenocarcinomas. Goblet cell carcinoids (GCCs) are uncommon neoplasms of the appendix that appear to be intermediate between carcinoid tumors and adenocarcinomas, both histologically and biologically. The current study was undertaken to examine the role of p53 and K-ras mutations in the pathogenesis of GCCs and typical carcinoids (TCs) of the appendix. METHODS. Archival materials from 22 GCCs and 18 TCs were analyzed. K-ras mutations in codons 12, 13, and 61 were studied by a polymerase chain reaction (PCR) based designed restriction fragment length polymorphism method using mismatched nested primers. Mutations in exons 5-8 of the p53 tumor suppressor gene were analyzed in 16 GCCs and 18 TCs by PCR and single-strand conformational polymorphism followed by direct sequencing. Immunostains for p53 and chromogranin were performed in all cases. RESULTS. K-ras mutations and nuclear accumulation of p53 by immunohistochemistry were not detected in any of the GCCs or TCs. p53 mutations were found in 4 of 16 GCCs (25{\%}) and 8 of 18 TCs (44{\%}). Immunoreactivity for chromogranin was seen in the vast majority of GCCs and TCs. CONCLUSIONS. p53 mutations appear to play a role in the pathogenesis of some GCCs and in approximately 50{\%} of TCs of the appendix, whereas mutations in the K-ras oncogene do not appear to be important in the development of these tumors. The minimal cytologic atypia, low incidence of metastases, and lack of K-ras mutations in goblet cell appendiceal neoplasms suggest that they are variants of carcinoid tumors. Our findings lend support to the recommendation that the therapeutic guidelines applied to TCs of the appendix should be the same for GCCs.",
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T1 - K-ras and p53 mutations in the pathogenesis of classical and goblet cell carcinoids of the appendix

AU - Ramnani, Dharam M.

AU - Wistuba, Ignacio I.

AU - Behrens, Carmen

AU - Gazdar, Adi F.

AU - Sobin, Leslie H.

AU - Albores-Saavedra, Jorge

PY - 1999/7/1

Y1 - 1999/7/1

N2 - BACKGROUND. Mutations in the K-ras oncogene and the p53 tumor suppressor gene are present in approximately 50% of colonic adenocarcinomas. Goblet cell carcinoids (GCCs) are uncommon neoplasms of the appendix that appear to be intermediate between carcinoid tumors and adenocarcinomas, both histologically and biologically. The current study was undertaken to examine the role of p53 and K-ras mutations in the pathogenesis of GCCs and typical carcinoids (TCs) of the appendix. METHODS. Archival materials from 22 GCCs and 18 TCs were analyzed. K-ras mutations in codons 12, 13, and 61 were studied by a polymerase chain reaction (PCR) based designed restriction fragment length polymorphism method using mismatched nested primers. Mutations in exons 5-8 of the p53 tumor suppressor gene were analyzed in 16 GCCs and 18 TCs by PCR and single-strand conformational polymorphism followed by direct sequencing. Immunostains for p53 and chromogranin were performed in all cases. RESULTS. K-ras mutations and nuclear accumulation of p53 by immunohistochemistry were not detected in any of the GCCs or TCs. p53 mutations were found in 4 of 16 GCCs (25%) and 8 of 18 TCs (44%). Immunoreactivity for chromogranin was seen in the vast majority of GCCs and TCs. CONCLUSIONS. p53 mutations appear to play a role in the pathogenesis of some GCCs and in approximately 50% of TCs of the appendix, whereas mutations in the K-ras oncogene do not appear to be important in the development of these tumors. The minimal cytologic atypia, low incidence of metastases, and lack of K-ras mutations in goblet cell appendiceal neoplasms suggest that they are variants of carcinoid tumors. Our findings lend support to the recommendation that the therapeutic guidelines applied to TCs of the appendix should be the same for GCCs.

AB - BACKGROUND. Mutations in the K-ras oncogene and the p53 tumor suppressor gene are present in approximately 50% of colonic adenocarcinomas. Goblet cell carcinoids (GCCs) are uncommon neoplasms of the appendix that appear to be intermediate between carcinoid tumors and adenocarcinomas, both histologically and biologically. The current study was undertaken to examine the role of p53 and K-ras mutations in the pathogenesis of GCCs and typical carcinoids (TCs) of the appendix. METHODS. Archival materials from 22 GCCs and 18 TCs were analyzed. K-ras mutations in codons 12, 13, and 61 were studied by a polymerase chain reaction (PCR) based designed restriction fragment length polymorphism method using mismatched nested primers. Mutations in exons 5-8 of the p53 tumor suppressor gene were analyzed in 16 GCCs and 18 TCs by PCR and single-strand conformational polymorphism followed by direct sequencing. Immunostains for p53 and chromogranin were performed in all cases. RESULTS. K-ras mutations and nuclear accumulation of p53 by immunohistochemistry were not detected in any of the GCCs or TCs. p53 mutations were found in 4 of 16 GCCs (25%) and 8 of 18 TCs (44%). Immunoreactivity for chromogranin was seen in the vast majority of GCCs and TCs. CONCLUSIONS. p53 mutations appear to play a role in the pathogenesis of some GCCs and in approximately 50% of TCs of the appendix, whereas mutations in the K-ras oncogene do not appear to be important in the development of these tumors. The minimal cytologic atypia, low incidence of metastases, and lack of K-ras mutations in goblet cell appendiceal neoplasms suggest that they are variants of carcinoid tumors. Our findings lend support to the recommendation that the therapeutic guidelines applied to TCs of the appendix should be the same for GCCs.

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