Expression of nm23-H1 gene product in thyroid, ovary, and breast cancers

Cell Biophysics
|June 1, 1995
PubMed

Insights

The nm23-H1 gene product, a key factor in cancer metastasis, was found to be reduced in metastatic lymph nodes. Its expression in primary tumors varied by cancer type, suggesting a role in metastasis for certain cancers.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • The nm23 gene product is implicated as a mediator of cancer invasion and metastasis.
  • Reduced nm23-H1 mRNA and protein levels are observed in metastatic lymph nodes of thyroid papillary carcinoma patients.

Purpose of the Study:

  • To investigate the expression of the nm23 gene product in various human cancers.
  • To determine the correlation between nm23-H1 expression and metastasis in thyroid, ovarian, and breast cancers.

Main Methods:

  • Immunohistochemistry was used to examine nm23-H1 and nm23-H2 gene product expression.
  • The study analyzed 115 thyroid cancers, 78 ovarian cancers, 63 breast cancers, and metastatic lymph node tissues.

Main Results:

  • nm23-H1, not nm23-H2, was expressed in primary thyroid, ovarian, and breast cancers (excluding medullary and anaplastic thyroid carcinomas).
  • Expression of nm23-H1 was weak or poor in metastatic lymph nodes across all cancer types studied.
  • Lower nm23-H1 expression was noted in anaplastic and medullary thyroid carcinomas, but no significant differences were found among histological types of ovarian and breast cancers.

Conclusions:

  • The nm23-H1 gene product may play a role in the metastasis of thyroid, ovarian, and breast cancers.
  • Other factors likely contribute to the metastasis of anaplastic and medullary thyroid carcinomas.