| Sample | Role of LRG1 | References |
---|---|---|---|
Biliary tract | Serum | In conjunction with CA19-9 and IL-6, particularly elevated in high-risk patients with primary sclerosing cholangitis | [179] |
Tumour tissue | Suggested as independent prognostic factor | [224] | |
Bladder | Urine | Suggested as biomarker for early diagnosis and monitoring of recurrence | [186] |
Breast | Tumour tissue | Suggested as biomarker for neo-adjuvant aromatase inhibitor treatment. Associated with number of lymphatic metastasis, tumour stage and poor survival | |
Cervical | Urine | Together with MMRN1, highly expressed in urines of cervical cancer patients | [227] |
Colorectal | Plasma | In conjunction with other biomarkers, proposed as predictive, diagnostic, and prognostic factor. Positively correlates with tumour stage and size | |
Serum | In conjunction with other biomarkers, suggested as diagnostic, prognostic, and follow-up factor. Associated with altered glycosylation | ||
Tumour tissue | Associated with cancer aggressiveness and vascular density. Proposed as diagnostic in general and prognostic for stage III colorectal cancer | ||
Stool | In conjunction with Hp, SYNE2, RBP4, FN1 and ANXA6, suggested for early detection of high-risk adenomas and colorectal cancer | [234] | |
Endometrial | Tumour tissue | Suggested as independent prognostic factor of stage and lymphatic metastasis | [235] |
Esophageal | Plasma | Significantly elevated in esophageal squamous cell carcinoma and, in conjunction with alpha-2-HS-glycoprotein, proposed as biomarker for early diagnosis | [236] |
Tumour tissue | Closely correlated with worse clinical survival | [237] | |
Serum | In combination with CRP and sIL-6R, suggested as biomarker to predict response to preoperative chemoradiotherapy | [238] | |
Gastric | Serum and tumour tissue | Proposed as prognostic factor. Promotes tumour progression and affects negatively patient relapse-free survival. Correlation between tissue scores and serum levels | [183] |
Glioblastoma | Plasma | In conjunction with CRP and C9, shows positive correlation with tumour size | [192] |
Tumour tissue | Significantly higher than in lower-grade glioma. Proposed as potential diagnostic, prognostic, and regional biomarker | [239] | |
Hepatocellular | Serum | Significantly elevated as part of a broad panel of protein biomarkers and associated with poor responders followig transarterial chemoembolization | |
Tumour tissue | Positive correlation with tumour size, differentiation, stage, vascularity. Negative correlation with patient survival | [181] | |
Leukemia | Serum | Highly expressed in acute lymphoblastic leukemia T and B cells. Suggested as biomarker for early diagnosis | |
Lung | Plasma | Significantly elevated in patients with non-small cell lung carcinoma and, in conjunction with ACT, C9 and Hpt, proposed as diagnostic factor. Highly indicative of reduced survival time post-radiotherapy | |
Serum | Significantly elevated and, in conjunction with SAA and C4BP, prognostic in patients with squamous cell lung carcinoma. Expressed by circulating tumour cells in metastatic patients | ||
Urine | Candidate biomarker for diagnosis of non-small cell lung carcinoma. Highly expressed in urinary exosomes | ||
Tumour tissue | Upregulated in non-small cell lung carcinoma | [190] | |
Oral | Plasma | In combination with apolipoprotein A-IV, suggested as biomarker for oral cancer screening and early diagnosis | [248] |
Serum | Increased in oral squamous cell carcinoma and suggested as early diagnostic tool with ABG, CLU, PRO2044, HAP, C3, proapo-A1 and RBP4 | [249] | |
Saliva | Significantly elevated in oral squamous cell carcinoma and, together with CFB, C3, C4B and SERPINA1, associated with increased risk | [250] | |
Ovarian | Serum | Alone or in combination with other biomarkers suggested as diagnostic factor | |
Urine | Multiple LRG1 peptides detected in the urines of all ovarian cancer patients | ||
Pancreatic | Plasma | Exceeds diagnostic performance of CA19-9 alone in the early detection of pancreatic ductal adenocarcinoma (PDAC). High levels distinguish PDAC from chronic pancreatitis. Elevated during formation of intraductal papillary mucinous neoplasm | |
Serum | In combination with CA19-9, suggested as diagnostic biomarker. Characterized with altered glycosylation pattern. Increases with clinical stage | ||
Tumour tissue | Associated with higher recurrence rate and worse recurrence-free survival | [256] | |
Prostate | Serum | Elevated in fatal prostate cancer. Positively correlated with high risk of disease progression and mortality | [260] |
Renal | Tumour tissue | Overexpressed in clear renal cell carcinoma and negatively related to patient survival | [261] |
Retinal | Tumour tissue | Highly expressed in retinoblastoma | [262] |