Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/119043
Author(s): Ferreira, JA
Peixoto, A
Neves, M
Gaiteiro, C
Reis, CA
Assaraf, Y
Santos, L
Title: Mechanisms of cisplatin resistance and targeting of cancer stem cells: Adding glycosylation to the equation
Publisher: Elsevier
Issue Date: 2016
Abstract: Cisplatin-based chemotherapeutic regimens are the most frequently used (neo)adjuvant treatments for the majority of solid tumors. While platinum-based chemotherapeutic regimens have proven effective against highly proliferative malignant tumors, significant relapse and progression rates as well as decreased overall survival are still observed. Currently, it is known that sub-populations of chemoresistant cells share biological properties with cancer stem cells (CSC), which are believed to be responsible for tumor relapse, invasion and ultimately disease dissemination through acquisition of mesenchymal cell traits. In spite of concentrated efforts devoted to decipher the mechanisms underlying CSC chemoresistance and to design targeted therapeutics to these cells, proteomics has failed to unveil molecular signatures capable of distinguishing between malignant and non-malignant stem cells. This has hampered substantial developments in this complex field. Envisaging a novel rationale for an effective therapy, the current review summarizes the main cellular and molecular mechanisms underlying cisplatin resistance and the impact of chemotherapy challenge in CSC selection and clinical outcome. It further emphasizes the growing amount of data supporting a role for protein glycosylation in drug resistance. The dynamic and context-dependent nature of protein glycosylation is also comprehensively discussed, hence highlighting its potentially important role as a biomarker of CSC. As the paradigm of cancer therapeutics shifts towards precision medicine and patient-tailored therapeutics, we bring into focus the need to introduce glycomics and glycoproteomics in holistic pan-omics models, in order to integrate diverse, multimodal and clinically relevant information towards more effective cancer therapeutics.
Subject: Antineoplastic Agents/pharmacology
Biomarkers, Tumor/metabolism
Cisplatin/pharmacology
Drug Resistance, Neoplasm/physiology
Glycosylation/drug effects
Humans
Neoplasms/drug therapy
Neoplasms/metabolism
Neoplasms/pathology
Neoplastic Stem Cells/drug effects
Neoplastic Stem Cells/metabolism
URI: https://hdl.handle.net/10216/119043
Source: Drug Resistance Updates, vol.24, p. 34-54
Related Information: info:eu-repo/grantAgreement/FCT/COMPETE/125428/PT
info:eu-repo/grantAgreement/FCT/COMPETE/132983/PT
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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