Advanced Science (Jun 2019)

A Novel Blood‐Based Colorectal Cancer Diagnostic Technology Using Electrical Detection of Colon Cancer Secreted Protein‐2

  • Minhong Jeun,
  • Hyo Jeong Lee,
  • Sungwook Park,
  • Eun‐ju Do,
  • Jaewon Choi,
  • You‐Na Sung,
  • Seung‐Mo Hong,
  • Sang‐Yeob Kim,
  • Dong‐Hee Kim,
  • Ja Young Kang,
  • Hye‐Nam Son,
  • Jinmyoung Joo,
  • Eun Mi Song,
  • Sung Wook Hwang,
  • Sang Hyoung Park,
  • Dong‐Hoon Yang,
  • Byong Duk Ye,
  • Jeong‐Sik Byeon,
  • Jaewon Choe,
  • Suk‐Kyun Yang,
  • Helen Moinova,
  • Sanford D. Markowitz,
  • Kwan Hyi Lee,
  • Seung‐Jae Myung

DOI
https://doi.org/10.1002/advs.201802115
Journal volume & issue
Vol. 6, no. 11
pp. n/a – n/a

Abstract

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Abstract Colorectal cancer (CRC) is the second‐leading cause of cancer‐related mortality worldwide, which may be effectively reduced by early screening. Colon cancer secreted protein‐2 (CCSP‐2) is a promising blood marker for CRC. An electric‐field effect colorectal sensor (E‐FECS), an ion‐sensitive field‐effect transistor under dual gate operation with nanostructure is developed, to quantify CCSP‐2 directly from patient blood samples. The sensing performance of the E‐FECS is verified in 7 controls and 7 CRC samples, and it is clinically validated on 30 controls, 30 advanced adenomas, and 81 CRC cases. The concentration of CCSP‐2 is significantly higher in plasma samples from CRC and advanced adenoma compared with controls (both P < 0.001). Sensitivity and specificity for CRC versus controls are 44.4% and 86.7%, respectively (AUC of 0.67), and 43.3% and 86.7%, respectively, for advanced adenomas (AUC of 0.67). CCSP‐2 detects a greater number of CRC cases than carcinoembryonic antigen does (45.6% vs 24.1%), and the combination of the two markers detects an even greater number of cases (53.2%). The E‐FECS system successfully detects CCSP‐2 in a wide range of samples including early stage cancers and advanced adenoma. CCSP‐2 has potential for use as a blood‐based biomarker for CRC.

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