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  • member
  • team
  • department
  • center
  • program_project
  • nrc
  • whocc
  • project
  • software
  • tool
  • patent
  • Administrative Staff
  • Assistant Professor
  • Associate Professor
  • Clinical Research Assistant
  • Clinical Research Nurse
  • Clinician Researcher
  • Department Manager
  • Dual-education Student
  • Full Professor
  • Honorary Professor
  • Lab assistant
  • Master Student
  • Non-permanent Researcher
  • Nursing Staff
  • Permanent Researcher
  • Pharmacist
  • PhD Student
  • Physician
  • Post-doc
  • Prize
  • Project Manager
  • Research Associate
  • Research Engineer
  • Retired scientist
  • Technician
  • Undergraduate Student
  • Veterinary
  • Visiting Scientist
  • Deputy Director of Center
  • Deputy Director of Department
  • Deputy Director of National Reference Center
  • Deputy Head of Facility
  • Director of Center
  • Director of Department
  • Director of Institute
  • Director of National Reference Center
  • Group Leader
  • Head of Facility
  • Head of Operations
  • Head of Structure
  • Honorary President of the Departement
  • Labex Coordinator
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Scientific Fields
Diseases
Organisms
Applications
Technique
Starting Date
01
Nov 2016
Ending Date
03
Feb 2020
Status
Completed
Members
15
Structures
7
Instituts
1

About

The Oncobiomics project is conducted in the HTE (heterogenity tumor ecosystem) national program launched by the cancer nation institute (Inca) in the third national cancer plan 2014-2019. It’s a consortium project involving 8 teams from 5 differents national institutions (academics and privates).
The goal of this national and interdisciplinary consortium is to define how inter-tumor heterogeneity and differences between cancer cells within a tumor can lead to variable response to therapies.
The consortium aims at deciphering how the interplay between the tumor microenvironment and its microbiome may contribute to tumor plasticity and/or tumor-immunosuppressive milieu that may promote emergence of resistances. To this end, a system biology approach with the two following complementary aims was envisaged i) defining bacterial, in situ metabolomic, immune and genetic signatures across stages of colorectal cancer progression and ii) identifying sequence of events leading to the tumoral heterogeneity in response to tumor-residing bacteria. To this end, a highly interdisciplinary translational program benefits from a continued fruitful collaborative research approach gathering complementary inputs on bacteriology, biostatistics, immunology, metagenomics and oncology, and expertise on the emerging role of the stromal microenvironment on cancer progression and acquired therapy resistance. Biomics involvement was transversal on all of these fields.

Fundings