Tavares Catarina, Coelho Maria João, Melo Miguel, da Rocha Adriana Gaspar, Pestana Ana, Batista Rui, Salgado Catarina, Eloy Catarina, Ferreira Luciana, Rios Elisabete, Sobrinho-Simões Manuel, Soares Paula
Instituto de Investigação e Inovação em Saúde, Universidade do Porto (i3S), University of Porto, Porto, Portugal; Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), University of Porto, Porto, Portugal; Medical Faculty, University of Porto, Porto, Portugal.
Instituto de Investigação e Inovação em Saúde, Universidade do Porto (i3S), University of Porto, Porto, Portugal; Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), University of Porto, Porto, Portugal; Institute of Biomedical Sciences of Abel Salazar of the University of Porto (ICBAS), Porto, Portugal.
Surgery. 2016 Dec;160(6):1582-1590. doi: 10.1016/j.surg.2016.06.050. Epub 2016 Aug 26.
Activation of the mTOR pathway has been observed in thyroid cancer, but the biologic consequences regarding tumor behavior and patient prognosis remain poorly explored.
We aimed to evaluate the associations of the mTOR pathway with clinicopathologic and molecular features and prognosis through the immunocharacterization of pmTOR and pS6 expression (as readouts of the pathway) in a series of 191 papillary thyroid carcinomas.
pmTOR expression was associated with distant metastases (P = .05) and persistence of disease (P = .05). Cases with greater expression of pmTOR were submitted to more I treatments (r[102] = 0.2; P = .02) and a greater cumulative dose of radioactive iodine (r[100] = 0.3; P = .01). Positive pmTOR expression showed to be an independent risk factor for distant metastases (odds ratio = 18.2; 95% confidence interval 2.1-157.9; P = .01). In contrast, pS6 expression was associated with absence of extrathyroid extension (P = .001), well-defined tumor margins (P = .05), and wild-type BRAF status (P = .01). There was no correlation between the expression of pmTOR and pS6 expression (r[140] = 0.1; P = .3).
pmTOR expression is an indicator of aggressive, metastatic papillary thyroid carcinoma, being possibly implicated in refractoriness to therapy, while pS6 expression is associated with less aggressive pathologic features. Further studies are needed to understand better the biologic consequences of activation of the mTOR pathway in the behavior of thyroid cancer, namely the contribution of other pmTOR downstream effectors.
在甲状腺癌中已观察到mTOR通路的激活,但关于肿瘤行为和患者预后的生物学后果仍未得到充分研究。
我们旨在通过对191例乳头状甲状腺癌中pmTOR和pS6表达(作为该通路的读数)进行免疫特征分析,评估mTOR通路与临床病理、分子特征及预后的相关性。
pmTOR表达与远处转移(P = 0.05)和疾病持续存在(P = 0.05)相关。pmTOR表达较高的病例接受了更多的碘治疗(r[102] = 0.2;P = 0.02)和更高的放射性碘累积剂量(r[100] = 0.3;P = 0.01)。pmTOR阳性表达是远处转移的独立危险因素(比值比 = 18.2;95%置信区间2.1 - 157.9;P = 0.01)。相比之下,pS6表达与无甲状腺外侵犯(P = 0.001)、肿瘤边界清晰(P = 0.05)和BRAF野生型状态(P = 0.01)相关。pmTOR表达与pS6表达之间无相关性(r[140] = 0.1;P = 0.3)。
pmTOR表达是侵袭性、转移性乳头状甲状腺癌的一个指标,可能与治疗难治性有关,而pS6表达与侵袭性较低的病理特征相关。需要进一步研究以更好地理解mTOR通路激活在甲状腺癌行为中的生物学后果,即其他pmTOR下游效应器的作用。