Distinct genetic aberrations in oesophageal adeno and squamous carcinoma

被引:19
|
作者
Pandilla, Ramaswamy [1 ]
Kotapalli, Viswakalyan [1 ]
Gowrishankar, Swarnalata [2 ]
Chigurupati, MohanaVamsy [3 ]
Patnaik, Sujith [3 ]
Uppin, Shantveer [4 ]
Rao, Subramanyeshwar [5 ,6 ]
Kalidindi, NarasimhaRaju [3 ]
Regulagadda, Sastry [4 ]
Sundaram, Challa [4 ]
Srinivasulu, Mukta [5 ,6 ]
Vasala, Anjayneyulu [5 ,6 ]
Bashyam, Murali Dharan [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost CDFD, Mol Oncol Lab, Hyderabad, Andhra Pradesh, India
[2] Apollo Hosp, Hyderabad, Andhra Pradesh, India
[3] Basavatarakam Indo Amer Canc Hosp & Res Inst, Hyderabad, Andhra Pradesh, India
[4] Nizams Inst Med Sci, Hyderabad, Andhra Pradesh, India
[5] MNJ Inst Oncol, Hyderabad, Andhra Pradesh, India
[6] Reg Canc Ctr, Hyderabad, Andhra Pradesh, India
关键词
Adenosquamous mixed cancers; EGFR; esophageal adenocarcinoma; esophageal squamous cell carcinoma; p53; Wnt; HIGH-INCIDENCE AREA; MICROSATELLITE INSTABILITY; BARRETTS-ESOPHAGUS; PROGNOSTIC-FACTORS; CELL CARCINOMAS; CANCER; EXPRESSION; MUTATION; ADENOCARCINOMA; ACCUMULATION;
D O I
10.1111/eci.12163
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe two main oesophageal cancer subtypes namely adenocarcinoma and squamous cell carcinoma exhibit interesting clinical, pathological and geographical variations with the former being more common in the West and the latter in Asia. Materials and methodsWe evaluated status of p53, EGFR, Wnt and HPV in addition to microsatellite instability and loss of heterozygosity of several chromosomal loci in the two oesophageal cancer subtypes from India. The comparative analysis was extended to two oesophageal adenosquamous mixed cancer samples. ResultsOur results reveal a high frequency of EGFR overexpression in ESCC as against EAC, while Wnt activation was a significantly more common event in EAC as against ESCC. Frequencies of p53 perturbations were not significantly different in the two subtypes. Interestingly, the EGFR and Wnt status in adenocarcinoma and squamous components of the two oesophageal adenosquamous cancer samples were identical to primary tumours. In addition, no common molecular aberration (including instability and loss of heterozygosity) in several microsatellites was detected in DNA isolated from the two components in both adenosquamous cancer samples. ConclusionsOur results reveal the presence of distinct aberrations in oesophageal adenocarcinoma and squamous cell carcinoma which are replicated in the respective components of adenosquamous cancers. The study therefore suggests perhaps an independent origin of the two components of oesophageal adenosquamous mixed cancer.
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收藏
页码:1233 / 1239
页数:7
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