2020
DOI: 10.1016/j.jpba.2020.113300
|View full text |Cite
|
Sign up to set email alerts
|

Proteomic Analysis of Metastasis-Specific Biomarkers in Pancreatic Cancer: Galectin-1 Plays an Important Metastatic Role in Pancreatic Cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
3
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(12 citation statements)
references
References 11 publications
0
3
0
Order By: Relevance
“…In SILAC-DDA MS method, PGAM1, cadherin-3 (CDH3), plasminogen activator urokinase (PLAU), and lunatic fringe (LFNG) were suggested as potential therapeutic target. [123,125] Leukemia inhibitory factor (LIF), LGALS1, TIMP1, ALDH1A1, and GSN were also discovered with therapeutic significance using PRM-based MS and MALDI-TOF MS. [118,124,132,133] Moreover, several proteins, including LGALS3BP, MMP2, CTSD, SERPINE1, BGN, TIMP2, and LGALS1, were identified as potential therapeutic targets, showcasing the proteome complexity in PDAC. [120]…”
Section: Ms-based Protein Biomarkers For Pdacmentioning
confidence: 99%
See 1 more Smart Citation
“…In SILAC-DDA MS method, PGAM1, cadherin-3 (CDH3), plasminogen activator urokinase (PLAU), and lunatic fringe (LFNG) were suggested as potential therapeutic target. [123,125] Leukemia inhibitory factor (LIF), LGALS1, TIMP1, ALDH1A1, and GSN were also discovered with therapeutic significance using PRM-based MS and MALDI-TOF MS. [118,124,132,133] Moreover, several proteins, including LGALS3BP, MMP2, CTSD, SERPINE1, BGN, TIMP2, and LGALS1, were identified as potential therapeutic targets, showcasing the proteome complexity in PDAC. [120]…”
Section: Ms-based Protein Biomarkers For Pdacmentioning
confidence: 99%
“…In SILAC-DDA MS method, PGAM1, cadherin-3 (CDH3), plasminogen activator urokinase (PLAU), and lunatic fringe (LFNG) were suggested as potential therapeutic target. [123,125] Leukemia inhibitory factor (LIF), LGALS1, TIMP1, ALDH1A1, and GSN were also discovered with therapeutic significance using PRM-based MS and MALDI-TOF MS. [118,124,132,133] Moreover, several proteins, including LGALS3BP, MMP2, CTSD, SERPINE1, BGN, TIMP2, and LGALS1, were identified as potential therapeutic targets, showcasing the proteome complexity in PDAC. [120] In the PTM level, Cao et al [119] uncovered potential therapeutic targets through phosphoproteomics analysis and identified glycoproteins for early detection in PDAC via TMT labeling, including sialyltransferase (ST6GAL1, ST3GAL1), fucosyltransferase (FUT3, FUT11), and galactosyltransferase (B4GALT4, B4GALT1).…”
Section: Prognostic Biomarkersmentioning
confidence: 99%
“…Galectin-1 expression in pancreatic cancer demonstrates a significant association with the disease's progression and metastasis, particularly in lymph node metastases [75]. Compared to normal pancreatic tissues, Gal-1 expression has been found to be substantially higher in both primary malignant tumors and metastatic tissues [75].…”
Section: Galectin-1 and Lymph Node Metastasis In Pancreatic Cancermentioning
confidence: 99%
“…Galectin-1 expression in pancreatic cancer demonstrates a significant association with the disease's progression and metastasis, particularly in lymph node metastases [75]. Compared to normal pancreatic tissues, Gal-1 expression has been found to be substantially higher in both primary malignant tumors and metastatic tissues [75]. This increase appears even more pronounced in advanced lymph node metastases, highlighting a potentially critical role for Gal-1 in pancreatic cancer's invasive nature [72,75].…”
Section: Galectin-1 and Lymph Node Metastasis In Pancreatic Cancermentioning
confidence: 99%
“…Galectin-1 (Gal1) is one of the 15 members of the beta-galactose-binding proteins, galactoagglutinins. Recent studies have demonstrated that Gal1 is expressed in a variety of malignant tumors, including hepatocellular carcinomas [ 7 ], lung adenocarcinomas [ 8 ], pancreatic cancers [ 9 ], breast cancers [ 10 ], colon cancers [ 11 ], and GC [ 12 ]. It is mainly distributed in the extracellular matrix and cytoplasm, and regulates various biological activities of cancer cells.…”
Section: Introductionmentioning
confidence: 99%