[Application of iPDMS protein microarray in screening of tumor-associated antigen autoantibodies]

Sheng Wu Gong Cheng Xue Bao. 2021 Nov 25;37(11):4075-4082. doi: 10.13345/j.cjb.210017.
[Article in Chinese]

Abstract

The rapid screening of tumor markers is a challenging task for early diagnosis of cancer. This study aims to use highly sensitive chemiluminescent protein microarray technology to efficiently screen a variety of low abundance tumor related markers. A new material, termed integrated polydimethylsiloxane modified silica gel (iPDMS), was obtained by adding a surface polymerization initiator with olefin end to the conventional polydimethylsiloxane, and fixing into the three-dimensional structure of polydimethylsiloxane by thermal crosslinking through silicon hydrogen bonding. In order to make the iPDMS material resistant to non-specific protein adsorption, a poly(OEGMA) polymer brush was synthesized by surface-initiated atom transfer radical polymerization at the active initiation site. Finally, 20 tumor-related antigens were printed into the specific areas of the microarray by high-throughput spray printing technology, and assembled into 48-well detection microtiterplates of the iPDMS microarray. It was found the VEGFR and VEGF121 autoantibodies that obtained from 8 common tumors (breast cancer, lung cancer, colon cancer, gastric cancer, liver cancer, leukemia, lymphoma and ovarian cancer) can be used as potential tumor markers. The chemiluminescence labeled iPDMS protein microarray can be used for the screening of tumor autoantibodies at early stage.

Keywords: VEGF121; VEGFR1; iPDMS protein microarray; tumor marker.

MeSH terms

  • Adsorption
  • Autoantibodies*
  • Dimethylpolysiloxanes
  • Protein Array Analysis*
  • Silica Gel
  • Surface Properties

Substances

  • Autoantibodies
  • Dimethylpolysiloxanes
  • Silica Gel