Bos R, Zhong H, Hanrahan C F, Mommers E C, Semenza G L, Pinedo H M, Abeloff M D, Simons J W, van Diest P J, van der Wall E
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
J Natl Cancer Inst. 2001 Feb 21;93(4):309-14. doi: 10.1093/jnci/93.4.309.
Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that regulates gene expression in critical pathways involved in tumor growth and metastases. In this report, we investigated whether the level of HIF-1 alpha is increased during carcinogenesis in breast tissue and is associated with other tumor biomarkers.
Paraffin-embedded clinical specimens from five pathologic stages of breast tumorigenesis and from normal breast tissue were used. HIF-1 alpha protein and the biomarkers vascular endothelial growth factor (VEGF), HER-2/neu, p53, Ki-67, and estrogen receptor (ER) were identified immunohistochemically, and microvessel density (a measure of angiogenesis) was determined. Associations among levels of HIF-1 alpha and these biomarkers were tested statistically. All statistical tests are two-sided.
The frequency of HIF-1 alpha-positive cells in a specimen increased with the specimen's pathologic stage (P<.001, chi(2) test for trend) as follows: normal breast tissue (0 specimens with > or = 1% HIF-1 alpha-positive cells in 10 specimens tested), ductal hyperplastic lesions (0 in 10), well-differentiated ductal carcinomas in situ (DCIS) (11 in 20), well-differentiated invasive breast cancers (12 in 20), poorly differentiated DCIS (17 in 20), and poorly differentiated invasive carcinomas (20 in 20). Increased levels of HIF-1 alpha were statistically significantly associated with high proliferation and increased expression of VEGF and ER proteins. In DCIS lesions, increased levels of HIF-1 alpha were statistically significantly associated with increased microvessel density. HIF-1alpha showed a borderline association with HER-2/neu but no association with p53.
The level of HIF-1 alpha increases as the pathologic stage increases and is higher in poorly differentiated lesions than in the corresponding type of well-differentiated lesions. Increased levels of HIF-1 alpha are associated with increased proliferation and increased expression of ER and VEGF. Thus, increased levels of HIF-1 alpha are potentially associated with more aggressive tumors.
缺氧诱导因子-1(HIF-1)是一种转录因子,可调节参与肿瘤生长和转移的关键途径中的基因表达。在本报告中,我们研究了乳腺组织癌变过程中HIF-1α水平是否升高,以及它是否与其他肿瘤生物标志物相关。
使用来自乳腺肿瘤发生的五个病理阶段以及正常乳腺组织的石蜡包埋临床标本。采用免疫组织化学方法鉴定HIF-1α蛋白以及生物标志物血管内皮生长因子(VEGF)、HER-2/neu、p53、Ki-67和雌激素受体(ER),并测定微血管密度(一种血管生成的指标)。对HIF-1α水平与这些生物标志物之间的关联进行统计学检验。所有统计检验均为双侧检验。
标本中HIF-1α阳性细胞的频率随标本的病理阶段增加而升高(P<0.001,趋势χ²检验),具体如下:正常乳腺组织(在10个检测标本中,0个标本有≥1%的HIF-1α阳性细胞)、导管增生性病变(10个中0个)、高分化导管原位癌(DCIS)(20个中11个)、高分化浸润性乳腺癌(20个中12个)、低分化DCIS(20个中17个)和低分化浸润性癌(20个中20个)。HIF-1α水平升高与高增殖以及VEGF和ER蛋白表达增加在统计学上显著相关。在DCIS病变中,HIF-1α水平升高与微血管密度增加在统计学上显著相关。HIF-1α与HER-2/neu呈临界关联,但与p53无关联。
HIF-1α水平随病理阶段增加而升高,在低分化病变中高于相应类型的高分化病变。HIF-1α水平升高与增殖增加以及ER和VEGF表达增加相关。因此,HIF-1α水平升高可能与更具侵袭性的肿瘤相关。