Cell-Free Circulating Methylated SEPT9 for Noninvasive Diagnosis and Monitoring of Colorectal Cancer.
Cell-Free Circulating Methylated SEPT9 for Noninvasive Diagnosis and Monitoring of Colorectal Cancer.
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无细胞循环甲基化 SEPT9 用于结直肠癌的无创诊断和监测
DOI:
10.1155/2018/6437104
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发表时间:
2018
期刊:
影响因子:
--
通讯作者:
Liu W
中科院分区:
文献类型:
--
作者:
Fu B;Yan P;Zhang S;Lu Y;Pan L;Tang W;Chen S;Chen S;Zhang A;Liu W
Identification of early-stage tumor and monitoring therapeutic efficacy and recurrence or metastasis of colorectal cancer (CRC) are urgently warranted for improving the outcome of CRC patients and reducing the disease-related mortality. In this study, we evaluated the diagnostic value of cell-free circulating methylated SEPT9 (mSEPT9) for CRC and beyond CRC and examined the potentiality of mSEPT9 in assessing therapeutic efficacy and monitoring recurrence of CRC. Our results confirmed the favorable diagnostic value of plasma mSEPT9 for CRC, with a sensitivity of 61.22% (95% confidence interval (CI): 51.33%–70.27%) and specificity of 93.7% (95% CI: 91.09%–95.57%) using 2/3 algorithm. The positive rate of mSEPT9 in CRC was correlated with tumor size, histological grade, and general histological type (P < 0.05). Beyond CRC, gastric cancer patients also presented a high positive rate of plasma mSEPT9 (70%). The conversions between preoperative and postoperative plasma mSEPT9 reflected the therapeutic efficacy of curatively intended surgery for CRC patients. The persistent positivity of plasma mSEPT9 after surgery (within 7–14 days) was highly associated with impending recurrences or metastases (within one year), with a sensitivity of 100%. Postoperative mSEPT9 status during follow-up also provided valuable indication for CRC recurrence or metastases, with a good consistency (kappa = 0.818, P = 0.001). Our results verified the reliability of plasma mSEPT9 as a biomarker for noninvasive diagnosis of CRC. More significantly, we revealed its valuable role in appraising CRC therapeutic efficacy and monitoring CRC recurrences or metastases. Further studies with larger sample sizes are needed to verify and elucidate the clinical utility of the promising findings.
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影响因子:
11
作者:
Al-Shuneigat JM;Mahgoub SS;Huq F
通讯作者:
Huq F
影响因子:
3.5
作者:
Mitchell SM;Ho T;Brown GS;Baker RT;Thomas ML;McEvoy A;Xu ZZ;Ross JP;Lockett TJ;Young GP;LaPointe LC;Pedersen SK;Molloy PL
通讯作者:
Molloy PL
影响因子:
4.6
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Ng SB;Chua C;Ng M;Gan A;Poon PS;Teo M;Fu C;Leow WQ;Lim KH;Chung A;Koo SL;Choo SP;Ho D;Rozen S;Tan P;Wong M;Burkholder WF;Tan IB
通讯作者:
Tan IB
影响因子:
2.9
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通讯作者:
Coleman MP
影响因子:
5
作者:
Lee, Hye Seung;Hwang, Sang Mee;Park, Kyoung Un
通讯作者:
Park, Kyoung Un