Pavithra V, Kumari Karuna, Haragannavar Vanishri C, Rao Roopa S, Nambiar Shwetha, Augustine Dominic, Sowmya S V
Postgraduate, Department of Oral Pathology, MS Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
Postgraduate, Department of Oral Pathology, M S Ramaiah University of Applied Sciences, Bengaluru, Karnataka, India.
J Clin Diagn Res. 2017 Sep;11(9):ZC51-ZC54. doi: 10.7860/JCDR/2017/29363.10601. Epub 2017 Sep 1.
Oral carcinoma is a global health problem. India accounts for one-third of world burden with high prevalence rate of 2.5 million and mortality rate of 5.5 lacs per year. Oral carcinogenesis is a multistage process that frequently involves invasion and metastasis that needs early detection and treatment to improve the overall quality of life. The ability of Oral Squamous Cell Carcinoma (OSCC) to metastasize to lymph nodes does not always show a relationship with clinical staging. A spectrum of molecular mechanisms is involved in carcinogenesis, where defect in the regulation of apoptosis is assumed to contribute to the pathogenesis and progression of cancer. Apoptosis regulatory genes include the antiapoptotic protein such as B-cell lymphoma-2 (Bcl-2) gene that might be used as a molecular marker to evaluate the biological behaviour of oral cancer.
To evaluate and correlate the Bcl-2 expression in OSCC patients with lymphnode metastasis and without metastasis.
The study comprised of 30 samples, 15 cases of metastatic and 15 non-metastatic primary OSCC. All the cases were stained for routine Hematoxylin and Eosin (H&E), and Bcl-2 antibody by immunohistochemistry. The H&E stained sections were evaluated for Lymphocytic Infiltrate (LI) and Pattern Of Invasion (POI). Bcl-2 stained sections were evaluated for staining intensity and distribution. The differences between the groups were statistically analysed using chi-square test.
The histopathological parameters, LI and POI did not show any statistical difference between the study groups. Expression of Bcl-2 in OSCC was 33.3% among the study groups, where metastatic group showed a positive expression of 13.3% and 20% in non-metastatic OSCC that did not show statistically significance among the study groups.
There was no significant difference in the expression of Bcl-2 between the study groups. Apoptosis is regulated by interaction among the Bcl-2 gene family. Hence, evaluation of Bcl-2 along with other apoptotic regulating proteins could define the role in pathogenesis and prognosis of metastatic and non-metastatic OSCC.
口腔癌是一个全球性的健康问题。印度占全球口腔癌负担的三分之一,患病率高达250万,每年死亡率为55万。口腔癌发生是一个多阶段过程,常涉及侵袭和转移,需要早期检测和治疗以提高总体生活质量。口腔鳞状细胞癌(OSCC)转移至淋巴结的能力并不总是与临床分期相关。一系列分子机制参与致癌过程,其中细胞凋亡调节缺陷被认为与癌症的发病机制和进展有关。细胞凋亡调节基因包括抗凋亡蛋白,如B细胞淋巴瘤-2(Bcl-2)基因,它可能用作评估口腔癌生物学行为的分子标志物。
评估并关联OSCC患者中伴有和不伴有淋巴结转移时Bcl-2的表达情况。
本研究包括30个样本,15例转移性原发性OSCC和15例非转移性原发性OSCC。所有病例均进行常规苏木精和伊红(H&E)染色,以及通过免疫组织化学检测Bcl-2抗体。对H&E染色切片评估淋巴细胞浸润(LI)和侵袭模式(POI)。对Bcl-2染色切片评估染色强度和分布。使用卡方检验对两组之间的差异进行统计学分析。
组织病理学参数LI和POI在研究组之间未显示出任何统计学差异。研究组中OSCC的Bcl-2表达为33.3%,其中转移组阳性表达为13.3%,非转移性OSCC为20%,在研究组之间未显示出统计学意义。
研究组之间Bcl-2的表达无显著差异。细胞凋亡受Bcl-2基因家族之间的相互作用调节。因此,评估Bcl-2以及其他凋亡调节蛋白可以确定其在转移性和非转移性OSCC的发病机制和预后中的作用。