Sundquist Elias, Kauppila Joonas H, Veijola Johanna, Mroueh Rayan, Lehenkari Petri, Laitinen Saara, Risteli Juha, Soini Ylermi, Kosma Veli-Matti, Sawazaki-Calone Iris, Macedo Carolina Carneiro Soares, Bloigu Risto, Coletta Ricardo D, Salo Tuula
Cancer and Translational Medicine Research Unit, University of Oulu, Oulu FI-90014, Finland.
Medical Research Centre, Oulu University Hospital, Oulu FI-90014, Finland.
Br J Cancer. 2017 Feb 28;116(5):640-648. doi: 10.1038/bjc.2016.455. Epub 2017 Jan 17.
Oral tongue squamous cell carcinoma (OTSCC) metastasises early, especially to regional lymph nodes. There is an ongoing debate on which early stage (T1-T2N0) patients should be treated with elective neck dissection. We need prognosticators for early stage tongue cancer.
Mice immunisation with human mesenchymal stromal cells resulted in production of antibodies against tenascin-C (TNC) and fibronectin (FN), which were used to stain 178 (98 early stage), oral tongue squamous cell carcinoma samples. Tenascin-C and FN expression in the stroma (negative, moderate or abundant) and tumour cells (negative or positive) were assessed. Similar staining was obtained using corresponding commercial antibodies.
Expression of TNC and FN in the stroma, but not in the tumour cells, proved to be excellent prognosticators both in all stages and in early stage cases. Among early stages, when stromal TNC was negative, the 5-year survival rate was 88%. Correspondingly, when FN was negative, no cancer deaths were observed. Five-year survival rates for abundant expression of TNC and FN were 43% and 25%, respectively.
Stromal TNC and, especially, FN expressions differentiate patients into low- and high-risk groups. Surgery alone of early stage primary tumours might be adequate when stromal FN is negative. Aggressive treatments should be considered when both TNC and FN are abundant.
口腔舌鳞状细胞癌(OTSCC)早期即发生转移,尤其是区域淋巴结转移。对于哪些早期(T1 - T2N0)患者应接受选择性颈清扫术,目前仍存在争议。我们需要早期舌癌的预后指标。
用人间充质基质细胞免疫小鼠,产生抗腱生蛋白-C(TNC)和纤连蛋白(FN)的抗体,用于对178例(98例早期)口腔舌鳞状细胞癌样本进行染色。评估基质(阴性、中度或丰富)和肿瘤细胞(阴性或阳性)中TNC和FN的表达情况。使用相应的商业抗体也获得了类似的染色结果。
TNC和FN在基质而非肿瘤细胞中的表达,在所有阶段及早期病例中均被证明是极佳的预后指标。在早期病例中,当基质TNC为阴性时,5年生存率为88%。相应地,当FN为阴性时,未观察到癌症死亡病例。TNC和FN丰富表达时的5年生存率分别为43%和25%。
基质TNC,尤其是FN的表达可将患者分为低风险和高风险组。当基质FN为阴性时,早期原发性肿瘤单独手术可能就足够了。当TNC和FN均丰富时,应考虑积极治疗。