Tetraspanin 8 (TSPAN 8) as a potential target for radio-immunotherapy of colorectal cancer

نویسندگان

  • Aurelie Maisonial-Besset
  • Tiffany Witkowski
  • Isabelle Navarro-Teulon
  • Odile Berthier-Vergnes
  • Giovanna Fois
  • Yingying Zhu
  • Sophie Besse
  • Olivia Bawa
  • Arnaud Briat
  • Mercedes Quintana
  • Alexandre Pichard
  • Mathilde Bonnet
  • Eric Rubinstein
  • Jean-Pierre Pouget
  • Paule Opolon
  • Lydia Maigne
  • Elisabeth Miot-Noirault
  • Jean-Michel Chezal
  • Claude Boucheix
  • Françoise Degoul
چکیده

Tetraspanin 8 (TSPAN8) overexpression is correlated with poor prognosis in human colorectal cancer (CRC). A murine mAb Ts29.2 specific for human TSPAN8 provided significant efficiency for immunotherapy in CRC pre-clinical models. We therefore evaluate the feasability of targeting TSPAN8 in CRC with radiolabeled Ts29.2. Staining of tissue micro-arrays with Ts29.2 revealed that TSPAN8 espression was restricted to a few human healthy tissues. DOTA-Ts29.2 was radiolabeled with 111In or 177Lu with radiochemical purities >95%, specific activity ranging from 300 to 600 MBq/mg, and radioimmunoreactive fractions >80%. The biodistribution of [111In]DOTA-Ts29.2 in nude mice bearing HT29 or SW480 CRC xenografts showed a high specificity of tumor localization with high tumor/blood ratios (HT29: 4.3; SW480-TSPAN8: 3.9 at 72h and 120h post injection respectively). Tumor-specific absorbed dose calculations for [177Lu]DOTA-Ts29.2 was 1.89 Gy/MBq, establishing the feasibility of using radioimmunotherapy of CRC with this radiolabeled antibody. A significant inhibition of tumor growth in HT29 tumor-bearing mice treated with [177Lu]DOTA-Ts29.2 was observed compared to control groups. Ex vivo experiments revealed specific DNA double strand breaks associated with cell apoptosis in [177Lu]DOTA-Ts29.2 treated tumors compared to controls. Overall, we provide a proof-of-concept for the use of [111In/177Lu]DOTA-Ts29.2 that specifically target in vivo aggressive TSPAN8-positive cells in CRC.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017