TY - JOUR
T1 - Lung cancer molecular mutations and abnormal glycosylation as biomarkers for early diagnosis
AU - Yang, Shuang
AU - Xia, Jun
AU - Yang, Zeren
AU - Xu, Mingming
AU - Li, Shuwei
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2021/1
Y1 - 2021/1
N2 - Lung cancer is the leading cause of mortality and morbidity in tumor-related deaths in the world. Early detection of tumors can greatly improve the survival rate of patients. However, the lack of reliable blood biomarkers remains a major challenge for early diagnosis. The blood proteins secreted by the lung bronchi and bronchial arteries may have characteristic glycosylation patterns associated with tumors, which are different from normal physiological and pathological conditions. In this review, we outline the oncogenic drivers, signaling pathways related to KRAS, gene and protein mutations, and oncogenic regulation of protein glycosylation. Based on to the TCGA transcriptomics and antibody-based proteomics data, we discussed oncogene and glycoproteins detected in the blood as tumor biomarkers. We hypothesize that glycoproteins whose glycosylation can be reversed by targeted drugs may serve as potential tumor biomarkers.
AB - Lung cancer is the leading cause of mortality and morbidity in tumor-related deaths in the world. Early detection of tumors can greatly improve the survival rate of patients. However, the lack of reliable blood biomarkers remains a major challenge for early diagnosis. The blood proteins secreted by the lung bronchi and bronchial arteries may have characteristic glycosylation patterns associated with tumors, which are different from normal physiological and pathological conditions. In this review, we outline the oncogenic drivers, signaling pathways related to KRAS, gene and protein mutations, and oncogenic regulation of protein glycosylation. Based on to the TCGA transcriptomics and antibody-based proteomics data, we discussed oncogene and glycoproteins detected in the blood as tumor biomarkers. We hypothesize that glycoproteins whose glycosylation can be reversed by targeted drugs may serve as potential tumor biomarkers.
UR - http://www.scopus.com/inward/record.url?scp=85100184433&partnerID=8YFLogxK
U2 - 10.1016/j.ctarc.2021.100311
DO - 10.1016/j.ctarc.2021.100311
M3 - Review article
C2 - 33465560
AN - SCOPUS:85100184433
SN - 2468-2942
VL - 27
JO - Cancer Treatment and Research Communications
JF - Cancer Treatment and Research Communications
M1 - 100311
ER -