Glycomic, Glycoproteomic, and Proteomic Profiling of Philippine Lung Cancer and Peritumoral Tissues: Case Series Study of Patients Stages I–III

Author:

Alvarez Michael Russelle12ORCID,Zhou Qingwen1ORCID,Tena Jennyfer1,Barboza Mariana13,Wong Maurice1ORCID,Xie Yixuan1ORCID,Lebrilla Carlito B.1ORCID,Cabanatan Michelle4ORCID,Barzaga Ma. Teresa45,Tan-Liu Nelia4,Heralde Francisco M.46,Serrano Luster2,Nacario Ruel C.2,Completo Gladys Cherisse2ORCID

Affiliation:

1. Department of Chemistry, University of California Davis, Davis, CA 95616, USA

2. Institute of Chemistry, University of the Philippines Los Baños, Laguna 4031, Philippines

3. Department of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA 95616, USA

4. Molecular Diagnostics and Cellular Therapeutics Laboratory, Lung Center of the Philippines, Quezon City 1100, Philippines

5. College of Medicine, De La Salle Health Sciences Institute, Cavite 4114, Philippines

6. College of Medicine, University of the Philippines Manila, Manila City 1000, Philippines

Abstract

Lung cancer is the leading cause of cancer death and non-small cell lung carcinoma (NSCLC) accounting for majority of lung cancers. Thus, it is important to find potential biomarkers, such as glycans and glycoproteins, which can be used as diagnostic tools against NSCLC. Here, the N-glycome, proteome, and N-glycosylation distribution maps of tumor and peritumoral tissues of Filipino lung cancer patients (n = 5) were characterized. We present several case studies with varying stages of cancer development (I−III), mutation status (EGFR, ALK), and biomarker expression based on a three-gene panel (CD133, KRT19, and MUC1). Although the profiles of each patient were unique, specific trends arose that correlated with the role of aberrant glycosylation in cancer progression. Specifically, we observed a general increase in the relative abundance of high-mannose and sialofucosylated N-glycans in tumor samples. Analysis of the glycan distribution per glycosite revealed that these sialofucosylated N-glycans were specifically attached to glycoproteins involved in key cellular processes, including metabolism, cell adhesion, and regulatory pathways. Protein expression profiles showed significant enrichment of dysregulated proteins involved in metabolism, adhesion, cell−ECM interactions, and N-linked glycosylation, supporting the protein glycosylation results. The present case series study provides the first demonstration of a multi-platform mass-spectrometric analysis specifically for Filipino lung cancer patients.

Funder

Philippine-California Advanced Research Institute

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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