Arch Pathol Lab Med 2004,128(7):765–70 PubMed 47 Bai YQ, Yamamo

Arch Pathol Lab Med. 2004,128(7):765–70.PubMed 47. Bai YQ, Yamamoto H, Akiyama Y, Tanaka H, Takizawa T, Koike M, Kenji Yagi O, Saitoh K, Takeshita K, Iwai T, Yuasa Y: Ectopic expression of homeodomain protein CDX2 in intestinal metaplasia and carcinomas of the stomach. Cancer Lett 2002,176(1):47–55. 8PubMedCrossRef 48. Seno H, Oshima M, Taniguchi MA, Usami #Dinaciclib mw randurls[1|1|,|CHEM1|]# K, Ishikawa TO, Chiba T, Taketo MM: CDX2 expression in the stomach with intestinal metaplasia and intestinal-type cancer: Prognostic implications. Int J Oncol 2002,21(4):769–74.PubMed 49.

Mizoshita T, Tsukamoto T, Inada K, Ogasawara N, Hirata A, Kato S, Joh T, Itoh M, Yamamura Y, Tatematsu M: Immunohistochemically detectable Cdx2 is present in intestinal phenotypic elements in early gastric cancers of both differentiated and undifferentiated

types, with no correlation to non-neoplastic surrounding mucosa. Pathol Int 2004,54(6):392–400.PubMedCrossRef 50. Zhou Y, Li N, Zhuang W, Liu GJ, Wu TX: P53 codon 72 polymorphism and gastric cancer: a meta-analysis of the literature. Int J Cancer 2007, 121:1481–6.PubMedCrossRef 51. Simon R, Altman DG: Statistical aspects of prognostic factor studies in oncology. Br J Cancer 1994, 69:979–85.PubMedCrossRef 52. Qu LS, Chen H, Kuai XL, Xu ZF, Jin F: Effects of interferon therapy on development of hepatocellular carcinoma in patients with hepatitis C-related cirrhosis: A meta-analysis of randomized controlled trials. Hepatol Res 2012, 42:782–9.PubMedCrossRef Competing interests The authors have Selleckchem PF299 declared that no competing interests exist. Authors’ contributions FBK, CL, WYW and WL contribute to acquisition of data and interpretation of data; XTW performed statistical analysis and drafted manuscript; YBX conceived

of the study and participated in the design of the study; QX was involved in experimental design, coordinating the experiments and manuscript preparation. All authors have read and approved the final version of the manuscrpt. XTW, FBK, CL, WYW and WL contributed equally to this article.”
“Background Glioblastoma multiforme (GBM, a grade IV glioma) is a mafosfamide primary brain tumor that is highly malignant, and the patients diagnosed with GBM remain poor prognosis despite implementation of intensive therapeutic strategies and clinical efforts. To date, the diagnosis of GBM before clinical treatment is mainly by computer tomography (CT) and nuclear magnetic resonance imaging (MRI). However, they are expensive and difficult to spread. Therefore, it is an urgent need to find new approaches to early diagnose GBM and monitor disease progress. MicroRNAs (miRNAs) are a large class of small non-coding RNAs that regulate gene expression at the post-transcriptional level [1].

Comments are closed.