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细胞周期进展抑制剂 Geminin 的过表达与三阴性乳腺癌的肿瘤干细胞样表型相关。

Overexpression of Cell Cycle Progression Inhibitor Geminin is Associated with Tumor Stem-Like Phenotype of Triple-Negative Breast Cancer.

机构信息

INT Fondazione Pascale, Naples, Italy.

出版信息

J Breast Cancer. 2012 Jun;15(2):162-71. doi: 10.4048/jbc.2012.15.2.162. Epub 2012 Jun 28.

DOI:10.4048/jbc.2012.15.2.162
PMID:22807933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3395739/
Abstract

PURPOSE

Triple-negative breast cancer, has a significant clinical relevance being associated with a shorter median time to relapse and death and does not respond to endocrine therapy or other available targeted agents. For this reason, identifying the molecular pathways associated with increased aggressiveness, for example the presence of stem cell populations within the tumor and alteration of genes associated with cell cycle regulation represents an important objective in the clinical research into this neoplasm.

METHODS

To investigate the role of cell cycle progression inhibitor Geminin in triple-negative breast cancers and its potential correlation with stem-like phenotype of this neoplasm, we used tissue microarray technology to build a specific triple-negative breast cancer tissue micro-array. Geminin and cancer stem cell marker CD133 expression was further investigated at the mRNA level for selected breast tumor samples through realtime polymerase chain reaction quantification.

RESULTS

Our results showed that CD133 expression was significantly associated to high Geminin expression (p=0.017), a strong association between Ki-67 and tumor grade (p=0.020) and an inverse association between Geminin expression and lymphonode metastases (p=0.058), and a trend of statistically significance between Geminin marker expression and survival of triple-negative breast cancer patients (p=0.076).

CONCLUSION

The strong association between the expression of CD133 and Geminin could be useful in molecular stratification of breast tumors and in particular of triple-negative breast cancers.

摘要

目的

三阴性乳腺癌具有重要的临床相关性,与较短的中位复发和死亡时间相关,并且对内分泌治疗或其他可用的靶向药物没有反应。因此,确定与侵袭性增加相关的分子途径,例如肿瘤内存在干细胞群体以及与细胞周期调节相关的基因改变,代表了对这种肿瘤进行临床研究的重要目标。

方法

为了研究细胞周期进展抑制剂 Geminin 在三阴性乳腺癌中的作用及其与这种肿瘤的干细胞样表型的潜在相关性,我们使用组织微阵列技术构建了一个特定的三阴性乳腺癌组织微阵列。通过实时聚合酶链反应定量,进一步研究了 Geminin 和癌症干细胞标志物 CD133 在选定的乳腺癌样本中的 mRNA 水平的表达。

结果

我们的结果表明,CD133 的表达与高 Geminin 表达显著相关(p=0.017),Ki-67 与肿瘤分级之间存在强烈关联(p=0.020),Geminin 表达与淋巴结转移之间存在负相关(p=0.058),并且 Geminin 标志物表达与三阴性乳腺癌患者的生存之间存在统计学意义上的趋势(p=0.076)。

结论

CD133 和 Geminin 的表达之间的强烈关联可能有助于对乳腺癌,特别是三阴性乳腺癌进行分子分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/5ef71b5f4398/jbc-15-162-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/83a73e8d9436/jbc-15-162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/b667d87182c1/jbc-15-162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/f412dd2e074c/jbc-15-162-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/de058ce2f5f4/jbc-15-162-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/5ef71b5f4398/jbc-15-162-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/83a73e8d9436/jbc-15-162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/b667d87182c1/jbc-15-162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/f412dd2e074c/jbc-15-162-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/de058ce2f5f4/jbc-15-162-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/3395739/5ef71b5f4398/jbc-15-162-g005.jpg

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The role of cancer stem cells (CD133(+)) in malignant gliomas.癌症干细胞(CD133(+))在恶性神经胶质瘤中的作用。
靶向 AXL 和 RAGE 预防 geminin 过表达诱导的三阴性乳腺癌转移。
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