MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1177/030089161209800625

Медицинская библиотека · Tumori · 2012

Rare somatic mutation of pro-apoptotic BAX and BAK genes in common human cancers.

Kim Min Sung, Kim Sung Soo, Yoo Nam Jin, Lee Sug Hyung

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

AIMS AND

BACKGROUND

BAX and BAK are both pro-apoptotic Bcl-2 proteins and are essential for the pathway of intrinsic apoptosis. Apoptosis in cancer cells is frequently inactivated by somatic mutations. The aim of the study was to see whether somatic mutations of BAX and BAK genes are characteristics of common human cancers.

METHODS

We analyzed somatic mutation of BAX and BAK genes in 47 gastric, 47 colorectal, 47 breast, 47 lung and 47 prostate carcinomas, and 47 acute leukemias by a polymerase chain reaction and single-strand conformation polymorphism assay.

RESULTS

We identified BAX gene mutations in one colon (2.1%) and three gastric (6.4%) cancers. All of the mutations were frameshift mutations in the G8 repeat sequences and were detected in cancers with high microsatellite instability (36.4%). There was no evidence of BAX mutation in the other cancers, nor was somatic mutation of the BAK gene detected in the cancers.

CONCLUSIONS

Our data indicate that somatic mutation of BAX and BAK genes are rare in the common cancers (besides the cancers with high microsatellite instability) and suggest that neither BAX nor BAK mutation may causally be implicated in their tumorigenesis.

Для цитирования: Kim Min Sung, Kim Sung Soo, Yoo Nam Jin, Lee Sug Hyung. Rare somatic mutation of pro-apoptotic BAX and BAK genes in common human cancers.. Tumori. 2012. DOI: 10.1177/030089161209800625.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.