Akt, protein kinase C, and mitogen-activated protein kinase phosphorylation status in head and neck squamous cell carcinoma

被引:18
作者
Tosi, L
Rinaldi, E
Carinci, F
Farina, A
Pastore, A
Pelucchi, S
Cassano, L
Evangelisti, R
Carinci, P
Volinia, S
机构
[1] Univ Ferrara, Dipartimento Morfol & Embriol, I-44100 Ferrara, Italy
[2] Ist Istol & Embriol, Bologna, Italy
[3] Univ Ferrara, Clin ORL, I-44100 Ferrara, Italy
[4] Univ Bologna, Ctr Genet Mol, Fdn Carisbo, Bologna, Italy
[5] TIGEM, Telethon Instv Genet & Med, Naples, Italy
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2005年 / 27卷 / 02期
关键词
protein kinases; head and neck squamous cell carcinoma; Akt; PIKC; MAPK;
D O I
10.1002/hed.20120
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. To detect epigenetic changes in head and neck squamous cell carcinoma (HNSCC) and between metastatic and nonmetastatic tumors, we performed a systematic phosphorylation screening on different protein kinases. Methods. The phosphorylation levels of the serine-threonine kinase Akt, of mitogen-activated protein kinase (MAPK), and of protein kinase C (PKC) beta and epsilon were measured in a series of 94 biopsy specimens, corresponding to 47 HNSCCs and paired controls taken from clinically uninvolved tissue of the same patients. Results. Akt and MAPK were significantly underphosphorylated (two-sided p < .004) in tumors, whereas PKCs showed no differences from control samples. Second, although in control tissue there was a significant correlation between phosphorylation levels of Akt, MAPK, and PKC (all two-sided p < .05), many correlated activations were lost in tumors and even more in lymph node-positive tumors. Finally, p44 MAPK and Akt pThr308 were phosphorylated in a coordinated fashion only in lymph node-positive tumors (two-sided p < .01). Conclusions. This novel evidence documents important changes in the phosphorylation program during cancer progression of HNSCC. (C) 2005 Wiley Periodicals, Inc. Head Neck 27: 130-137, 2005
引用
收藏
页码:130 / 137
页数:8
相关论文
共 46 条
  • [1] Albanell J, 2001, CANCER RES, V61, P6500
  • [2] Bancroft CC, 2001, CLIN CANCER RES, V7, P435
  • [3] Increased MAPK activity and MKP-1 overexpression in human gastric adenocarcinoma
    Bang, YJ
    Kwon, JH
    Kang, SH
    Kim, JW
    Yang, YC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (01) : 43 - 47
  • [4] A specific function for phosphatidylinositol 3-kinase α (p85α-p110α) in cell survival and for phosphatidylinositol 3-kinase β (p85α-p110β) in de novo DNA synthesis of human colon carcinoma cells
    Bénistant, C
    Chapuis, H
    Roche, S
    [J]. ONCOGENE, 2000, 19 (44) : 5083 - 5090
  • [5] Oncogenic kinase signalling
    Blume-Jensen, P
    Hunter, T
    [J]. NATURE, 2001, 411 (6835) : 355 - 365
  • [6] Protein kinase c isoenzyme patterns characteristically modulated in early prostate cancer
    Cornford, P
    Evans, J
    Dodson, A
    Parsons, K
    Woolfenden, A
    Neoptolemos, J
    Foster, CS
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (01) : 137 - 144
  • [7] Activation of SAPK/JNK by camptothecin sensitizes androgen-independent prostate cancer cells to Fas-induced apoptosis
    Costa-Pereira, AP
    McKenna, SL
    Cotter, TG
    [J]. BRITISH JOURNAL OF CANCER, 2000, 82 (11) : 1827 - 1834
  • [8] Serine/threonine protein kinases and apoptosis
    Cross, TG
    Scheel-Toellner, D
    Henriquez, NV
    Deacon, E
    Salmon, M
    Lord, JM
    [J]. EXPERIMENTAL CELL RESEARCH, 2000, 256 (01) : 34 - 41
  • [9] Morphodensitometric analysis of protein kinase C βII expression in rat colon:: modulation by diet and relation to in situ cell proliferation and apoptosis
    Davidson, LA
    Brown, RE
    Chang, WCL
    Morris, JS
    Wang, NY
    Carroll, RJ
    Turner, ND
    Lupton, JR
    Chapkin, RS
    [J]. CARCINOGENESIS, 2000, 21 (08) : 1513 - 1519
  • [10] Ding Y, 2000, INT J ONCOL, V17, P695