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Cancer Biomarkers: Section A of Disease Markers logoLink to Cancer Biomarkers: Section A of Disease Markers
. 2013 Oct 31;13(4):299–305. doi: 10.3233/CBM-130352

Expression of PI3K, PTEN and Akt in small intestinal adenocarcinoma detected by quantum dots-based immunofluorescence technology

Yi Zhang a,1, Xue Yao a,1, Congqing Jiang b, Junqiu Yue c, Jing Guan d, Honglei Cheng a, Mohammed Hajirashid a, Yan Wang a, Lifang Fan a,*
PMCID: PMC12928286  PMID: 24240591

Abstract

Background:

Small intestinal adenocarcinoma (SIA) is often diagnosed at an advanced stage due to its rarity and nonspecific clinical manifestations. Abnormal activation of the PI3K/Akt pathway may lead to various diseases including cancer. In this study, we explored the relationship between those pathways and SIA.

Objective:

To investigate the expression of PI3K, phospho-Akt (p-Akt) and PTEN in SIA to evaluate their clinical significance.

Methods:

Expression of PI3K, p-Akt and PTEN biomarkers were examined by quantum dots-based immunofluorescence histochemistry (QDs-IHC) and traditional immunohistochemistry (IHC). There are 53 SIA samples, 11 non-cancer tissue samples and 11 normal small intestine tissues.

Results:

The positive frequencies of PI3K and p-Akt expression were significantly higher in the SIA group (77.4%, 41/53 and 77.4%, 41/53, respectively) than that in the non-cancer group (36.4%, 4/11 and 27.3, 3/11, respectively) and normal small intestine tissue group (36.4%, 4/11 and 18.2, 2/11, respectively). However, the difference of the positive rates of PTEN expression in three groups did not reach a statistical difference (P=0.761). The IHC results were in concordance with the QDs-IHC.

Conclusions:

These observations support that PI3K/Akt pathway is highly activated in SIA, which may implicate therapeutic targeting of the PI3K/Akt signaling pathway for its treatment.

Keywords: Adenocarcinoma, PI3K, PTEN, p-Akt, quantum dots, small intestine

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Articles from Cancer Biomarkers: Section A of Disease Markers are provided here courtesy of SAGE Publications

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