中國醫學科學院腫瘤研究所赫捷教授與清華大學郭永副研究員合作利用microRNA芯片系統的比較了60對肺鱗癌和癌旁組織microRNA表達譜的差異,發現了一個包含5個microRNA的分類器(hsa-miR-210,
hsa-miR-182, hsa-miR-486-5p, hsa-miR-30a and
hsa-miR-140-3p)。該分類器區分肺鱗癌和正常肺組織的準確率超過94%。與此同時,他們還發現hsa-miR-31的表達量與病人的存活期負相關。DICER1基因是hsa-miR-31的靶基因。
上述研究的博奧生物晶芯?哺乳動物miRNA芯片服務與Real time RT-PCR服務在博奧生物有限公司完成。
原文摘要:
A 5-MicroRNA Signature for Lung Squamous Cell Carcinoma Diagnosis and hsa-miR-31 for Prognosis Purpose:
Recent studies have suggested that microRNA biomarkers could be useful
for stratifying lung cancer subtypes, but microRNA signatures varied
between different populations. Squamous cell carcinoma (SCC) is one
major subtype of lung cancer that urgently needs biomarkers to aid
patient management. Here, we undertook the first comprehensive
investigation on microRNA in Chinese SCC patients. Experimental
Design: MicroRNA expression was measured in cancerous and noncancerous
tissue pairs strictly collected from Chinese SCC patients (stages
I–III), who had not been treated with chemotherapy or radiotherapy prior
to surgery. The molecular targets of proposed microRNA were further
examined.
Results: We identified a 5-microRNA
classifier (hsa-miR-210, hsa-miR-182, hsa-miR-486-5p, hsa-miR-30a, and
hsa-miR-140-3p) that could distinguish SCC from normal lung tissues. The
classifier had an accuracy of 94.1% in a training cohort (34 patients)
and 96.2% in a test cohort (26 patients). We also showed that high
expression of hsa-miR-31 was associated with poor survival in these 60
SCC patients by Kaplan–Meier analysis (P = 0.007), by univariate Cox
analysis (P = 0.011), and by multivariate Cox analysis (P = 0.011). This
association was independently validated in a separate cohort of 88 SCC
patients (P = 0.008, 0.011, and 0.003 in Kaplan–Meier analysis,
univariate Cox analysis, and multivariate Cox analysis, respectively).
We then determined that the tumor suppressor DICER1 is a target of
hsa-miR-31. Expression of hsa-miR-31 in a human lung cancer cell line
repressed DICER1 activity but not PPP2R2A or LATS2.
Conclusions: Our results identified a new
diagnostic microRNA classifier for SCC among Chinese patients and a new
prognostic biomarker, hsa-miR-31.