Mutation analysis of the gene encoding the human mannose 6-phosphate/insulin-like growth factor 2 receptor

A Gemma1, Y Hosoya, K Uematsu

  • 1Fourth Department of Internal Medicine, Nippon Medical School, Main Hospital, 1-1-5 Sendagi Bunkyo-ku, Tokyo 113-8602, Japan. gemma_akihiko/med4@nms.ac.jp

Insights

The mannose 6-phosphate/insulin-like growth factor 2 receptor (M6P/IGF2R) gene, a tumor suppressor, was analyzed for mutations in lung cancer. A novel M6P/IGF2R mutation was identified in lung adenocarcinoma, suggesting its role in lung carcinogenesis.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • The mannose 6-phosphate/insulin-like growth factor 2 receptor (M6P/IGF2R) gene functions in cell growth regulation and is implicated as a tumor suppressor.
  • Mutations and deletions in M6P/IGF2R have been observed in various human cancers.

Purpose of the Study:

  • To investigate the genomic structure of the M6P/IGF2R gene and develop primers for mutation detection.
  • To analyze M6P/IGF2R gene mutations in human cell lines resistant to TGF-beta(1) growth inhibition, particularly focusing on lung cancer.

Main Methods:

  • Designed intron primers for the 48-exon M6P/IGF2R gene.
  • Utilized polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and direct sequencing to analyze M6P/IGF2R coding sequences.
  • Screened 21 human cell lines resistant to TGF-beta(1).

Main Results:

  • Identified a previously reported mutation (adenine-to-guanine transition, Asn-to-Ser substitution) in exon 40 of M6P/IGF2R in one lung adenocarcinoma cell line.
  • This represents the first documented mutation of the M6P/IGF2R gene in a lung tumor.
  • The mutation was found in a cell line resistant to TGF-beta(1) mediated growth inhibition.

Conclusions:

  • The identified mutation in the M6P/IGF2R gene in lung adenocarcinoma suggests its potential involvement in human lung carcinogenesis.
  • Further investigation into M6P/IGF2R mutations is warranted for understanding their role in cancer development.

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