Application of C. elegans cancer screening test for the detection of pancreatic tumor in genetically engineered mice
Pancreatic ductal adenocarcinoma (PDAC) exhibits a very early onset of metastasis. Thus, early detection and treatment are pivotal to successful eradication of pancreatic cancers. Economical and non-invasive cancer screening systems is indispensable for this purpose. Previously our group developed a...
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Veröffentlicht in: | Oncotarget 2019-09, Vol.10 (52), p.5412-5418 |
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Sprache: | eng |
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Zusammenfassung: | Pancreatic ductal adenocarcinoma (PDAC) exhibits a very early onset of metastasis. Thus, early detection and treatment are pivotal to successful eradication of pancreatic cancers. Economical and non-invasive cancer screening systems is indispensable for this purpose. Previously our group developed a novel method to detect various kinds of human cancer using nematode
Caenorhabditis elegans (C. elegans)
that respond to cancer odor in urine; however, whether this method is useful for non-human species remains to be understood. In this study, we examined its effectiveness in the detection of murine pancreatic tumor spontaneously generated in genetically-engineered mice. We generated pancreas-specific
Kras
G12D
and/or
c-Met
deletion mutant mice and measured the probability of spontaneous tumor generation in these mice. The chemotactic indexes of
C. elegans
to the urine samples of these mutant mice were measured. As previously described, oncogenic
Kras
G12D
was necessary to induce pancreatic intraepithelial neoplasia in this mouse model, while c
-Met
mutation did not show further effect. The chemotactic analysis indicated that
C. elegans
avoids urine of healthy recipient mice, while they tended to be attracted to urine of mice with
Kras
G12D
. Our study demonstrated that
C. elegans
can recognize the odor of pancreatic cancer in urine of
Kras
G12D
model mouse, suggesting the similarity of cancer odor between species. Our result facilitates further studies on mechanism of cancer detection by
C. elegans
. |
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ISSN: | 1949-2553 1949-2553 |
DOI: | 10.18632/oncotarget.27124 |