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  Distinct nitrogen isotopic compositions of healthy and cancerous tissue in mice brain and head&neck micro-biopsies

Straub, M., Sigman, D. M., Auderset, A., Ollivier, J., Petit, B., Hinnenberg, B., et al. (2021). Distinct nitrogen isotopic compositions of healthy and cancerous tissue in mice brain and head&neck micro-biopsies. BMC Cancer, 21: 805. doi:10.1186/s12885-021-08489-x.

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 Creators:
Straub, M., Author
Sigman, D. M., Author
Auderset, A., Author
Ollivier, J., Author
Petit, B., Author
Hinnenberg, B., Author
Rubach, F., Author
Oleynik, S., Author
Vozenin, M.-C., Author
Martinez-Garcia, A.1, Author           
Affiliations:
1Climate Geochemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_2237635              

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 Abstract: Background

Cancerous cells can recycle metabolic ammonium for their growth. As this ammonium has a low nitrogen isotope ratio (15N/14N), its recycling may cause cancer tissue to have lower 15N/14N than surrounding healthy tissue. We investigated whether, within a given tissue type in individual mice, tumoral and healthy tissues could be distinguished based on their 15N/14N.
Methods

Micro-biopsies of murine tumors and adjacent tissues were analyzed for 15N/14N using novel high-sensitivity methods. Isotopic analysis was pursued in Nude and C57BL/6 mice models with mature orthotopic brain and head&neck tumors generated by implantation of H454 and MEERL95 murine cells, respectively.
Results

In the 7 mice analyzed, the brain tumors had distinctly lower 15N/14N than healthy neural tissue. In the 5 mice with head&neck tumors, the difference was smaller and more variable. This was at least partly due to infiltration of healthy head&neck tissue by tumor cells. However, it may also indicate that the 15N/14N difference between tumoral and healthy tissue depends on the nitrogen metabolism of the healthy organ in question.
Conclusions

The findings, coupled with the high sensitivity of the 15N/14N measurement method used here, suggest a new approach for micro-biopsy-based diagnosis of malignancy as well as an avenue for investigation of cancer metabolism.

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Language(s): eng - English
 Dates: 2021-07-13
 Publication Status: Published online
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 Identifiers: DOI: 10.1186/s12885-021-08489-x
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Title: BMC Cancer
Source Genre: Journal
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Pages: 13 Volume / Issue: 21 Sequence Number: 805 Start / End Page: - Identifier: -