Abstract

Background: Previous studies reported that stress-induced phosphoprotein 1 (STIP1) can be secreted by hepatocellular carcinoma (HCC) cells and is increased in the serum of HCC patients. However, the therapy-monitoring and prognostic value of serum STIP1 in HCC remains unclear. Here, we aimed to systemically explore the prognostic significance of serum STIP1 in HCC.Methods: A total of 340 HCC patients were recruited to this study; 161 underwent curative resection and 179 underwent transcatheter arterial chemoembolization (TACE). Serum STIP1 was detected by enzyme-linked immunosorbent assay (ELISA). Optimal cutoff values for serum STIP1 in resection and TACE groups were determined by receiver operating characteristic (ROC) analysis. Prognostic value was assessed by Kaplan-Meier, log-rank, and Cox regression analyses. Predictive values of STIP1 for objective response (OR) to TACE and MVI were evaluated by ROC curves and logistic regression.Results: Serum STIP1 was significantly increased in HCC patients when compared with chronic hepatitis B patients or health donors (both P < 0.05). Optimal cutoff values for STIP1 in resection and TACE groups were 83.43 and 112.06 ng/ml, respectively. High pretreatment STIP1 was identified as an independent prognosticator. Dynamic changes in high STIP1 status were significantly associated with long-term prognosis, regardless of treatment approaches. Moreover, post-TACE STIP1 was identified as an independent predictor for OR, with a higher area under ROC curve (AUC-ROC) than other clinicopathological features. Specifically, pretreatment STIP1 was significantly increased in patients with microvascular invasion (MVI), and was confirmed as a novel, powerful predictor for MVI.Conclusions: Serum STIP1 is a promising biomarker for outcome evaluation, therapeutic response assessment, and MVI prediction in HCC. Integration serum STIP1 detection into HCC management might facilitate early clinical decision making to improve the prognosis of HCC.

Highlights

  • Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies worldwide, with increasing incidence and mortality rates [1,2,3]

  • 517 individuals were recruited in the present study (HCC, 340; chronic hepatitis B, 55; healthy donors, 122, FIGURE 2 | Serum stress-induced phosphoprotein 1 (STIP1) was elevated in HCC and associated with tumor progression. (A) Distributions of serum STIP1 in HCC patients received curative resection (n = 161) and transcatheter arterial chemoembolization (TACE) (n = 179)

  • Mean age was 53.38 years for the resection group and 50.25 years for the TACE group, and 16.15% of patients in the resection group were female while 11.73% of patients in the TACE group were female

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Summary

Introduction

Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies worldwide, with increasing incidence and mortality rates [1,2,3]. Despite impressive innovations in surgical procedures, the overall survival (OS) of HCC patients remains unsatisfactory due to high incidence of recurrence or relapse after surgery [4,5,6]. Previous studies reported that stress-induced phosphoprotein 1 (STIP1) can be secreted by hepatocellular carcinoma (HCC) cells and is increased in the serum of HCC patients. The therapy-monitoring and prognostic value of serum STIP1 in HCC remains unclear. We aimed to systemically explore the prognostic significance of serum STIP1 in HCC

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