Jazii Ferdous-Rastgar, Najafi Zahra, Malekzadeh Reza, Conrads Thomas-P, Ziaee Abed-Ali, Abnet Christian, Yazdznbod Mansour, Karkhane Ali-Asghar, Salekdeh Ghasem-H
National Institute of Genetic Engineering and Biotechnology, PO BOX 14155 6343, Tehran, Iran.
World J Gastroenterol. 2006 Nov 28;12(44):7104-12. doi: 10.3748/wjg.v12.i44.7104.
To assess the proteome of normal versus tumor tissue in squamous cell carcinoma of the esophagus (SCCE) in Iranian patients and compare our results with former reports by using proteomics.
Protein was extracted from normal and tumor tissues. Two dimensional electrophoresis was carried out and spots with differential expression were identified with mass spectrometry. RNA extraction and RT-PCR along with immunodetection were performed.
Fourteen proteins were found whose expression levels differed in tumor compared to normal tissues. Mass spectrometric analysis resulted in the identification of beta-tropomyosin (TMbeta), myosin light chain 2 (and its isoform), myosin regulatory light chain 2, peroxyredoxin 2, annexin I and an unknown polypeptide as the down regulated polypeptides in tumor tissue. Heat shock protein 70 (HSP70), TPM4-ALK fusion oncoprotein 2, myosin light polypeptide 6, keratin I, GH16431p and calreticulin were the up-regulated polypeptides found in tumor tissue. Several of these proteins, such as TMbeta, HSP70, annexin I, calreticulin, TPM4-ALK and isoforms of myosins, have been well recognized in tumorigenesis of esophageal or other types of cancers.
Our study not only supports the involvement of some of the formerly reported proteins in SCCE but also introduces additional proteins found to be lost in SCCE, including TMbeta.
评估伊朗患者食管鳞状细胞癌(SCCE)中正常组织与肿瘤组织的蛋白质组,并通过蛋白质组学将我们的结果与以前的报告进行比较。
从正常组织和肿瘤组织中提取蛋白质。进行二维电泳,并用质谱法鉴定差异表达的斑点。进行RNA提取、RT-PCR以及免疫检测。
发现14种蛋白质在肿瘤组织中的表达水平与正常组织不同。质谱分析鉴定出β-原肌球蛋白(TMβ)、肌球蛋白轻链2(及其异构体)、肌球蛋白调节轻链2、过氧化物还原酶2、膜联蛋白I和一种未知多肽为肿瘤组织中下调的多肽。热休克蛋白70(HSP70)、TPM4-ALK融合癌蛋白2、肌球蛋白轻多肽6、角蛋白I、GH16431p和钙网蛋白是在肿瘤组织中上调的多肽。这些蛋白质中的几种,如TMβ、HSP70、膜联蛋白I、钙网蛋白、TPM4-ALK和肌球蛋白异构体,在食管癌或其他类型癌症的肿瘤发生中已得到充分认识。
我们的研究不仅支持了一些先前报道的蛋白质参与SCCE,还引入了在SCCE中发现缺失的其他蛋白质,包括TMβ。