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[人原发性非小细胞肺癌中因易位导致的C-myc激活]

[C-myc activation by translocation in human primary non-small cell lung cancer].

作者信息

Lu Y, Cheng S, Guo S

机构信息

Cancer Institute, CAMS & PUMC, Beijing.

出版信息

Zhonghua Yi Xue Za Zhi. 1996 Apr;76(4):275-7.

PMID:8758273
Abstract

OBJECTIVE

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.

METHODS

We applied major fluorescence in situ hybridization (FISH) in combination with immunohistochemistry.

RESULTS

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.

CONCLUSION

These results suggest that c-myc can be activated by translocation in human primary lung cancer.

摘要

目的

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。

方法

我们应用主要荧光原位杂交(FISH)结合免疫组织化学。

结果

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。

结论

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。

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