RETRACTED: Frequent genetic and biochemical alterations of the PI3-K/AKT/PTEN pathway in head and neck squamous cell carcinoma (Retracted Article)

被引:208
作者
Pedrero, JMG
Carracedo, DG
Pinto, CM
Zapatero, AH
Rodrigo, JP
Nieto, CS
Gonzalez, MV
机构
[1] Univ Oviedo, Unidad Oncol Quirurg, IUOPA Fac Med Oviedo, Oviedo 33006, Asturias, Spain
[2] Hosp Cent Asturias, Serv Otorrinolaringol, Oviedo, Asturias, Spain
[3] Hosp Cent Asturias, Serv Anat Patol, Oviedo, Asturias, Spain
关键词
head and neck squamous cell carcinoma; PTEN; PIK3CA; AKT2;
D O I
10.1002/ijc.20711
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the status of the PI 3-kinase/AKT/PTEN signaling pathway in a series of 117 head and neck squamous cell carcinomas (HNSCC) in a search for molecular alterations in genes/ proteins with potential prognostic value. For this purpose, PIK3CA and AKT2 gene amplification was assessed by multiplex and Quantitative Real-Time PCR. Protein expression of AKT, p-AKT, p110alpha and PTEN was determined by Western blot. PTEN allelic loss was evaluated by microsatellite analysis. PTEN-exon 5 was screened for point mutations by PCR-SSCP. Homozygous deletions were determined by multiplex PCR. PIK3CA gene was amplified in 43/117 (37%) fresh tumor samples, a frequency that did not differ from that found in archival premalignant tissues: 15/38 (39%); 12/40 (30%) fresh tumors harbored AKT2 gene amplification. AKT was found activated in 6/36 (17%) fresh tumor samples, when compared to their normal tissue counterparts. Of these 6 cases, 1 showed p110a overexpression and 5 displayed PTEN protein downregulation. Neither allelic loss (found in 11/77 informative cases) nor point mutations or homozygous deletions accounted for the reduced PTEN protein expression observed in our tumor series. The histologically normal mucosa of 4 patients displayed some of the molecular alterations analyzed. Dysregulation of the PI 3-K/AKT/PTEN pathway might contribute to early HNSCC tumorigenesis and might constitute a potential clinical target. Overall, 17/36 (47%) cases showed at least 1 of the molecular alterations studied here, which makes the PI 3-kinase-initiated signaling pathway one of the most frequently altered in HNSCC. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:242 / 248
页数:7
相关论文
共 36 条
[1]   The catalytic subunit of phosphoinositide 3-kinase: Requirements for oncogenicity [J].
Aoki, M ;
Schetter, C ;
Himly, M ;
Batista, O ;
Chang, HW ;
Vogt, PK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6267-6275
[2]   MOLECULAR ALTERATIONS OF THE AKT2 ONCOGENE IN OVARIAN AND BREAST CARCINOMAS [J].
BELLACOSA, A ;
DEFEO, D ;
GODWIN, AK ;
BELL, DW ;
CHENG, JQ ;
ALTOMARE, DA ;
WAN, MH ;
DUBEAU, L ;
SCAMBIA, G ;
MASCIULLO, V ;
FERRANDINA, G ;
PANICI, PB ;
MANCUSO, S ;
NERI, G ;
TESTA, JR .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (04) :280-285
[3]   Genetic imbalances with impact on survival in head and neck cancer patients [J].
Bockmühl, U ;
Schlüns, K ;
Küchler, I ;
Petersen, S ;
Petersen, I .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :369-375
[4]  
Bockmuhl U, 1996, CANCER RES, V56, P5325
[5]  
Bockmuhl U, 1997, CANCER RES, V57, P5213
[6]  
Califano J, 1996, CANCER RES, V56, P2488
[7]   New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase AKT pathway [J].
Cantley, LC ;
Neel, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4240-4245
[8]   Homozygous deletion of the PTEN tumor-suppressor gene is not a feature in oral squamous cell carcinoma [J].
Chen, Q ;
Samaranayake, LP ;
Zhou, H ;
Xiao, L .
ORAL ONCOLOGY, 2000, 36 (01) :95-99
[9]   Amplification of AKT2 in human pancreatic cancer cells and inhibition of ATK2 expression and tumorigenicity by antisense RNA [J].
Cheng, JQ ;
Ruggeri, B ;
Klein, WM ;
Sonoda, G ;
Altomare, DA ;
Watson, DK ;
Testa, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3636-3641
[10]   Pten is essential for embryonic development and tumour suppression [J].
Di Cristofano, A ;
Pesce, B ;
Cordon-Cardo, C ;
Pandolfi, PP .
NATURE GENETICS, 1998, 19 (04) :348-355