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DOI 10.1158/1078-0432.ccr-07-1041

Медицинская библиотека · Clinical cancer research : an official journal of the American Association for Cancer Research · 2007

Dissecting the Akt/mammalian target of rapamycin signaling network: emerging results from the head and neck cancer tissue array initiative.

Molinolo Alfredo A, Hewitt Stephen M, Amornphimoltham Panomwat, Keelawat Somboon, Rangdaeng Samraeung, Meneses García Abelardo, Raimondi Ana R, Jufe Rafael, Itoiz María, Gao Yan, Saranath Dhananjaya, Kaleebi George S, Yoo George H, Leak Lee, Myers Ernest M, Shintani Satoru, Wong David, Massey H Davis, Yeudall W Andrew, Lonardo Fulvio, Ensley John, Gutkind J Silvio

СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralПеревод в очереди

Аннотация

PURPOSE: As an approach to evaluate the expression pattern and status of activation of signaling pathways in clinical specimens from head and neck squamous cell carcinoma (HNSCC) patients, we established the Head and Neck Cancer Tissue Array Initiative, an international consortium aimed at developing a high-density HNSCC tissue microarray, with a high representation of oral squamous cell carcinoma.

EXPERIMENTAL

DESIGN

These tissue arrays were constructed by acquiring cylindrical biopsies from multiple individual tumor tissues and transferring them into tissue microarray blocks. From a total of 1,300 cases, 547 cores, including controls, were selected and used to build the array.

RESULTS

Emerging information by the use of phosphospecific antibodies detecting the activated state of signaling molecules indicates that the Akt-mammalian target of rapamycin (mTOR) pathway is frequently activated in HNSCC, but independently from the activation of epidermal growth factor receptor or the detection of mutant p53. Indeed, we identified a large group of tissue samples displaying active Akt and mTOR in the absence of epidermal growth factor receptor activation. Furthermore, we have also identified a small subgroup of patients in which the mTOR pathway is activated but not Akt, suggesting the existence of an Akt-independent signaling route stimulating mTOR.

CONCLUSIONS

These findings provide important information about the nature of the dysregulated signaling networks in HNSCC and may also provide the rationale for the future development of novel mechanism-based therapies for HNSCC patients.

Для цитирования: Molinolo Alfredo A, Hewitt Stephen M, Amornphimoltham Panomwat, Keelawat Somboon, Rangdaeng Samraeung, Meneses García Abelardo, Raimondi Ana R, Jufe Rafael, Itoiz María, Gao Yan, Saranath Dhananjaya, Kaleebi George S, Yoo George H, Leak Lee, Myers Ernest M, Shintani Satoru, Wong David, Massey H Davis, Yeudall W Andrew, Lonardo Fulvio, Ensley John, Gutkind J Silvio. Dissecting the Akt/mammalian target of rapamycin signaling network: emerging results from the head and neck cancer tissue array initiative.. Clinical cancer research : an official journal of the American Association for Cancer Research. 2007. DOI: 10.1158/1078-0432.ccr-07-1041.

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