Lu Y, Cheng S, Guo S
Cancer Institute, CAMS & PUMC, Beijing.
Zhonghua Yi Xue Za Zhi. 1996 Apr;76(4):275-7.
Lung cancer is one of the most common human neoplasms. The carcinogenesis and development of lung cancer are related to activation and inactivation of many oncogenes and tumor-suppressor genes. We reported c-myc activation by translocation in SV40T-transformed human bronchial epithelial cells and lung cancer cell line before. In order to confirm that c-myc translocation exists in human primary non-small cell lung cancer, we continued our studies in 12 primary human lung cancers.
We applied major fluorescence in situ hybridization (FISH) in combination with immunohistochemistry.
c-myc translocation was detected in two cases of the 12 primary lung cancers. Overexpression of c-myc was detected in the two cases by means of immunohistochemistry.
These results suggest that c-myc can be activated by translocation in human primary lung cancer.
肺癌是人类最常见的肿瘤之一。肺癌的发生和发展与许多癌基因和肿瘤抑制基因的激活与失活有关。我们之前报道过在SV40T转化的人支气管上皮细胞和肺癌细胞系中c-myc通过易位被激活。为了证实c-myc易位存在于人类原发性非小细胞肺癌中,我们对12例原发性人类肺癌继续进行了研究。
我们应用主要荧光原位杂交(FISH)结合免疫组织化学。
在12例原发性肺癌中的2例检测到c-myc易位。通过免疫组织化学在这2例中检测到c-myc的过表达。
这些结果表明c-myc在人类原发性肺癌中可通过易位被激活。