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Journal of Gastrointestinal & Digestive System | ISSN: 2161-069X | Volume: 8
&
&
October 29-30, 2018 | San Francisco, USA
International Conference on
Gastrointestinal Cancer and Therapeutics
4
th
World Congress on
Digestive & Metabolic Diseases
26
th
Annual Congress on
Cancer Science and Targeted Therapies
The role of microbiome perturbations in colorectal cancer: Diagnostic, therapeutic or both?
Manasi S Shah
University of Texas School of Public Health, USA
T
here is encouraging evidence for using a stool-based composite microbial non-invasive diagnostic for colorectal cancer.
Through our meta-analysis, we analyzed eight global cohorts, re-analyzing the raw 16S rRNA gene sequencing data to find
consistent biomarkers such as
Parvimonas micra, Fusobacterium
sp. and
Streptococcus anginosus
robust to demographic and
technical heterogeneity across the studies. We further evaluated which microbial markers in colorectal cancer tissue biopsy,
directly at the disease interfacewere consistently elevated across cohorts, the extent towhich theywere detectable in fecal samples
from the same colorectal cancer case and the pathways through which they might operate. We noticed OTUs elongated to genus
Parvimonas, Fusobacterium
and
Streptococcus
elevated in biopsies as well. Inferred functional analysis identified differences in
amino acid and lipid metabolism, likely driven by the altered abundances of
Fusobacterium, Leptotrichia, Enterobacteriaceae,
Comamonadaceae and Ruminococcaceae
. While promising, to be truly generalizable for the public, a microbial diagnostic for
colorectal cancer must overcome challenges in terms of confounding the microbial signal by other co-existing morbidities such
obesity, type-2 diabetes, and IBD or the intake of over-the-counter or prescribed medications which is known to influence the
gut microbial content. Along with diagnostic avenues,
in vivo
studies have characterized Wnt-β-catenin signaling cross-talks
with microbial communities and host immune system and can be causal in inflammation-driven colorectal cancer. Recent
studies have demonstrated that the immune-modulator effectiveness of CTLA-4 and PD-PDL1 based therapy is microbiota
dependent and lays ground to prove the utility of microbiome modulated immunotherapy for all cancers.
Biography
Manasi S Shah has completed her PhD from the University of Texas School of Public Health. She then worked briefly with Second Genome Inc., as a consultant and
is a current postdoctoral study from Stanford University School of Medicine. Currently working as a Staff Bioinformatics Scientist at Thermo Fisher Scientific, Manasi
has authored a couple of microbiomes focused papers and is currently working on a grant award she received to improve the Axiom microbiome array capabilities.
manasishah86@gmail.comManasi S Shah, J Gastrointest Dig Syst 2018, Volume 8
DOI: 10.4172/2161-069X-C8-085