Literature DB >> 19783881

Prognostic value of serum osteopontin in hepatocellular carcinoma patients treated with transarterial chemoembolization.

Sung Hoon Kim1, Young Hwa Chung, Soo Hyun Yang, Jeong A Kim, Myoung Kuk Jang, Sung Eun Kim, Danbi Lee, Sae Hwan Lee, Don Lee, Kang Mo Kim, Young Suk Lim, Han Chu Lee, Yung Sang Lee, Dong Jin Suh.   

Abstract

BACKGROUND/AIMS: Osteopontin (OPN) is overexpressed in hepatocellular carcinoma (HCC) with postoperative recurrence or extrahepatic metastasis. However, its prognostic value in patients treated with transarterial chemoembolization (TACE) is unclear. We investigated the utility of serum OPN levels and changes therein as prognostic markers in HCC patients who have received TACE.
METHODS: Forty-six patients with HCC were enrolled. Serum OPN levels were measured before and 4 weeks after TACE. Serum biochemistry and computed tomography (CT) scans were analyzed. We evaluated baseline serum OPN levels and subsequent changes therein in relation to tumor responses and cumulative survival rates following TACE. A decreasing pattern was defined as a decrease after TACE of more than 10% relative to baseline levels. A "responder" was defined as a patient who exhibited a tumor necrosis rate of higher than 50% on the follow-up CT scan.
RESULTS: Higher initial serum OPN levels were associated with a large tumor, portal vein invasion, and an advanced tumor stage. Patients who had lower initial serum OPN levels and those who exhibited decreasing patterns after TACE tended to have more favorable tumor responses (P=0.043 and 0.055, respectively) and exhibited better cumulative survival rates (P=0.036 and 0.030, respectively). However, the initial serum OPN level and subsequent changes in serum OPN levels were not independent predictors for survival on multivariate analysis.
CONCLUSIONS: Serum OPN levels were significantly higher in patients with advanced HCC. In addition, HCC patients with low pretreatment serum OPN levels and those for whom serum OPN declined following TACE exhibited better tumor responses and survived for longer.

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Year:  2009        PMID: 19783881     DOI: 10.3350/kjhep.2009.15.3.320

Source DB:  PubMed          Journal:  Korean J Hepatol        ISSN: 1738-222X


  6 in total

Review 1.  Circulating biomarkers of hepatocellular carcinoma response after locoregional treatments: New insights.

Authors:  Maria Tampaki; Polyxeni P Doumba; Melanie Deutsch; John Koskinas
Journal:  World J Hepatol       Date:  2015-07-18

Review 2.  Osteopontin as potential biomarker and therapeutic target in gastric and liver cancers.

Authors:  Dong-Xing Cao; Zhi-Jie Li; Xiao-Ou Jiang; Yick Liang Lum; Ester Khin; Nikki P Lee; Guo-Hao Wu; John M Luk
Journal:  World J Gastroenterol       Date:  2012-08-14       Impact factor: 5.742

Review 3.  Tumor Biomarkers and Interventional Oncology: Impact on Local Outcomes for Liver and Lung Malignancy.

Authors:  Yuan-Mao Lin; Ryosuke Taiji; Marco Calandri; Bruno C Odisio
Journal:  Curr Oncol Rep       Date:  2021-04-15       Impact factor: 5.075

Review 4.  ARD1/NAA10 in hepatocellular carcinoma: pathways and clinical implications.

Authors:  Danbi Lee; Myoung-Kuk Jang; Ji Hae Seo; Soo Hyung Ryu; Jeong A Kim; Young-Hwa Chung
Journal:  Exp Mol Med       Date:  2018-07-27       Impact factor: 8.718

Review 5.  Prognostic value of osteopontin in patients with hepatocellular carcinoma: A systematic review and meta-analysis.

Authors:  Tingting Sun; Peng Li; Diwen Sun; Qingao Bu; Guoqiang Li
Journal:  Medicine (Baltimore)       Date:  2018-10       Impact factor: 1.817

6.  Higher Matrix Stiffness Upregulates Osteopontin Expression in Hepatocellular Carcinoma Cells Mediated by Integrin β1/GSK3β/β-Catenin Signaling Pathway.

Authors:  Yang You; Qiongdan Zheng; Yinying Dong; Yaohui Wang; Lan Zhang; Tongchun Xue; Xiaoying Xie; Chao Hu; Zhiming Wang; Rongxin Chen; Yanhong Wang; Jiefeng Cui; Zhenggang Ren
Journal:  PLoS One       Date:  2015-08-17       Impact factor: 3.240

  6 in total

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