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. 2013 May;15(5):461–471. doi: 10.1593/neo.121024

Figure 2.

Figure 2

Evaluation for PTEN and proteins in the PI3K/mTOR pathways in HNSCC samples. (A) HNSCC TMA slides (NIDCR) were analyzed for PTEN (IHC). PTEN immunoreactivity in the tissue array cores (n = 347) was classified into five groups: 0 (less than 10% stained cells), 1 (10–25%), 2 (25–50%), 3 (50–75%), and 4 (75–100%). (B) PTEN levels in well-differentiated (wd), moderately differentiated (md), and poorly differentiated (pd) tumors. Scores were represented as average of PTEN stain per differentiation group (error bar, SEM; ***P ≤ .001). Poorly differentiated tumors (pd) express significantly lower levels of PTEN than well-differentiated (wd) or moderately differentiated carcinomas (md). (C) Heat map generated from the IHC analysis of the indicated proteins in the tissue microarray. Unsupervised clustering analysis shows correlation between pAKTSer473, pS6, EGFR, pAKTThr308, and PTEN. Separation of clusters was indicated for the groups in which PTEN and pEGFR are co-expressed (A), whereas cluster A1 defines a subgroup of HNSCC lesions in which both proteins are decreased.