Sialyl-Tn identifies muscle-invasive bladder cancer basal and luminal subtypes facing decreased survival, being expressed by circulating tumor cells and metastases

被引:37
作者
Lima, Luis [1 ,6 ,15 ,19 ]
Neves, Manuel [1 ,2 ]
Oliveira, Marta I. [3 ]
Dieguez, Lorena [3 ]
Freitas, Rui [4 ]
Azevedo, Rita [1 ,2 ]
Gaiteiro, Cristiana [1 ,2 ]
Soares, Janine [1 ]
Ferreira, Dylan [1 ]
Peixoto, Andreia [1 ,2 ,5 ,6 ]
Fernandes, Elisabete [1 ,2 ,6 ,7 ]
Montezuma, Diana [8 ]
Tavares, Ana [1 ,8 ]
Ribeiro, Ricardo [6 ,9 ,10 ,11 ,12 ]
Castro, Ana [13 ]
Oliveira, Manuel [14 ]
Fraga, Avelino [14 ]
Reis, Celso A. [2 ,6 ,15 ,16 ]
Santos, Lucio Lara [1 ,17 ,18 ]
Ferreira, Jose Alexandre [1 ,2 ,3 ,6 ,15 ,19 ]
机构
[1] Portuguese Inst Oncol, Expt Pathol & Therapeut Grp, Res Ctr, Oporto, Portugal
[2] Univ Porto, Abel Salazar Inst Biomed Sci, Oporto, Portugal
[3] Int Iberian Nanotechnol Lab, Braga, Portugal
[4] Portuguese Inst Oncol, Dept Urol, Oporto, Portugal
[5] INEB Inst Biomed Engn, New Therapies Grp, Oporto, Portugal
[6] Univ Porto, Inst Res & Innovat Hlth, Oporto, Portugal
[7] INEB Inst Biomed Engn, Biomat Multistage Drug & Cell Delivery, Oporto, Portugal
[8] Portuguese Inst Oncol Porto, Dept Pathol, Oporto, Portugal
[9] INEB Inst Biomed Engn, Tumour & Microenvironm Interact, Oporto, Portugal
[10] Univ Lisbon, Genet Lab, Fac Med, Lisbon, Portugal
[11] Ctr Hosp & Univ Coimbra, Dept Clin Pathol, Coimbra, Portugal
[12] Portuguese Inst Oncol, Mol Oncol Grp, Oporto, Portugal
[13] Hosp Santo Antonio, Porto Hosp Ctr, Dept Med Oncol, Oporto, Portugal
[14] Hosp Santo Antonio, Porto Hosp Ctr, Dept Urol, Oporto, Portugal
[15] Univ Porto IPATIMUP, Inst Mol Pathol & Immunol, Glycobiol Canc, Oporto, Portugal
[16] Univ Porto, Dept Pathol & Oncol, Fac Med, Oporto, Portugal
[17] Univ Fernando Pessoa, Hlth Sch, Oporto, Portugal
[18] Portuguese Inst Oncol, Dept Surg Oncol, Oporto, Portugal
[19] Porto Comprehens Canc Ctr, Oporto, Portugal
关键词
Bladder cancer subtypes; Sialyl-Tn; Predictive profile; Glycosylation; Circulating tumor cells; PHENOTYPE; ANTIGEN;
D O I
10.1016/j.urolonc.2017.08.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To evaluate the potential of sialyl-Tn (STn), a cancer-associated glycan antigen present in membrane glycoproteins, to improve a recent molecular model for stratification and prognostication of advanced stage bladder tumors based on keratins (KRT14, 5, and 20) expression. In addition, determine the association between STn and disease dissemination based on the evaluation of circulating tumor cells (CTCs) and the metastasis, which is a critical matter to improve patient management. Patients and methods: A retrospective series of 80 muscle-invasive primary bladder tumors and associated metastasis were screened for KRT14, 5, and 20 and STn by real-time polymerase chain reaction and immunohistochemistry. Peripheral blood was collected in a patients' subset, CTCs were isolated through a size-based microfluidic chip and screened for KRTs and STn. Results: Basal-like lesions presented worse cancer-specific and disease-free survival compared to luminal tumors. STn antigen inclusion discriminated patients with worst survival in each subgroup (P = 0.047 for luminal; P = 0.027 for basal-like tumors). STn expression in CTCs and distant metastasis was also demonstrated. Conclusion: This work reinforces the potential of the KRT-based model for bladder cancer management and the association of STn with aggressiveness, supporting its inclusion in predictive molecular models toward patient-tailored precision medicine. Moreover, we describe for the first time that CTCs and the metastasis present a basal phenotype and express the STn antigen, highlighting its link with disease dissemination. Future studies should focus on determining the biological and clinical significance of these observations in the context of liquid biopsies. Given the membrane nature of STn, highly specific targeted therapeutics may also be envisaged. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:675.e1 / 675.e8
页数:8
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