Temel Metin, Turkmen Arif, Dokuyucu Recep, Cevik Cengiz, Oztuzcu Serdar, Cengiz Beyhan, Mutaf Mehmet
Department of Plastic and Reconstructive Surgery, School of Medicine, Mustafa Kemal University, Hatay, Turkey,
Tumour Biol. 2015 Jun;36(6):4611-6. doi: 10.1007/s13277-015-3108-9. Epub 2015 Jan 23.
In loss of heterozygosity (LOH) studies at the chromosome 4q22-35 region, it was shown that the amount of deletion was high in basal cell carcinoma (BCC). It has been proposed that genes located in this chromosomal region could be tumor suppressor genes in BCC. It has been thought that deletions in the ING2 gene located in the same region can play a role in the pathophysiology of BCC and that deletions occurring in this region may influence the level of ING2 expression in BCC. Tumoral and non-tumoral tissues from 75 patients with BCC (45 men and 30 women) were included to the study. Lesions were excised by a surgical margin of 0.5 cm. After excision, RNA was isolated from tumoral and non-tumoral tissue samples. ING2 messenger RNA (mRNA) expression level was determined in tumoral and non-tumoral tissues by the real-time polymerase chain reaction (RT-PCR). It was detected that ING2 mRNA expression level decreased in tumoral tissues when compared to non-tumoral tissues from BCC patients (p = 0.0001). It was found that expression levels of this gene were comparable among patients with primary, recurrent, or multiple BCC. It is thought that ING2 gene expression level could contribute to the development of BCC but not be associated with the stage and the prognosis of the tumor.
在对4q22 - 35染色体区域进行的杂合性缺失(LOH)研究中发现,基底细胞癌(BCC)中该区域的缺失量很高。有人提出,位于该染色体区域的基因可能是BCC中的肿瘤抑制基因。人们认为,位于同一区域的ING2基因缺失可能在BCC的病理生理学中起作用,并且该区域发生的缺失可能会影响BCC中ING2的表达水平。本研究纳入了75例BCC患者(45例男性和30例女性)的肿瘤组织和非肿瘤组织。病变组织以0.5 cm的手术切缘切除。切除后,从肿瘤组织和非肿瘤组织样本中分离RNA。通过实时聚合酶链反应(RT-PCR)测定肿瘤组织和非肿瘤组织中ING2信使核糖核酸(mRNA)的表达水平。结果发现,与BCC患者的非肿瘤组织相比,肿瘤组织中ING2 mRNA表达水平降低(p = 0.0001)。还发现,该基因在原发性、复发性或多发性BCC患者中的表达水平相当。研究认为,ING2基因表达水平可能有助于BCC的发生发展,但与肿瘤的分期和预后无关。