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Analysis of collagen presence in brain tumors using spontaneous Raman scattering spectroscopy

https://doi.org/10.24931/2413-9432-2026-15-3-21-29

Abstract

As brain tumors progress, excess collagen increases the rigidity of the extracellular matrix, which promotes metastasis, impedes drug penetration, and reduces the effectiveness of therapy. A detailed study of collagen as a promising biomarker of malignancy is highly relevant for complementing histopathology for accurate diagnosis and treatment planning. This study proposes an approach to detect collagen in intracranial tumor tissues using spontaneous Raman spectroscopy with excitation at a wavelength 785 nm.

About the Authors

E. D. Antipova
Prokhorov General Physics Institute of Russian Academy of Sciences
Russian Federation

Moscow



I. D. Romanishkin
Prokhorov General Physics Institute of Russian Academy of Sciences
Russian Federation

Moscow



T. A. Savelieva
Prokhorov General Physics Institute of Russian Academy of Sciences; National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)
Russian Federation

Moscow



A. V. Ryabova
Prokhorov General Physics Institute of Russian Academy of Sciences; National Research Nuclear University MEPhI (Moscow Engineering Physics Institute); RUDN University
Russian Federation

Moscow



S. V. Shugay
N.N. Burdenko National Medical Research Center of Neurosurgery
Russian Federation

Moscow



A. V. Kosyrkova
N.N. Burdenko National Medical Research Center of Neurosurgery
Russian Federation

Moscow



G. V. Pavlova
N.N. Burdenko National Medical Research Center of Neurosurgery; Institute of Higher Nervous Activity and Neurophysiology of the Russian Academy of Sciences
Russian Federation

Moscow



I. N. Pronin
N.N. Burdenko National Medical Research Center of Neurosurgery
Russian Federation

Moscow



V. B. Loschenov
Prokhorov General Physics Institute of Russian Academy of Sciences; National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)
Russian Federation

Moscow



References

1. Chakraborty R., Asthana A., Singh A.K., Adhikari R., Bin Hasan A. Chapter 20 - Collagen - a highly developed and abundant fibrous protein: synthesis and characterization. Handbook of Natural Polymers, Elsevier, 2023, pp. 489-508. ISBN 9780323998536. doi: 10.1016/B978-0-323-99853-6.00013-9.

2. Naomi R., Ridzuan P.M., Bahari H. Current Insights into Collagen Type I. Polymers (Basel), 2021, vol. 16, pp. 2642. doi: 10.3390/polym13162642

3. Mohiuddin E., Wakimoto H. Extracellular matrix in glioblastoma: opportunities for emerging therapeutic approaches. American Journal of Cancer Research, 2021, vol. 11, pp. 3742–3754.

4. Di Vito A., Donato A., Bria J., Conforti F., La Torre D., Malara N., Donato G. Extracellular Matrix Structure and Interaction with Immune Cells in Adult Astrocytic Tumors. Cell Mol Neurobiol, 2024, vol. 1, pp. 54. doi: 10.1007/s10571-024-01488-z

5. Ge H., Tian M., Pei Q., Tan F., Pei H. Extracellular matrix stiffness: new areas affecting cell metabolism. Front Oncol, 2021, vol. 11, pp. 631991. doi: 10.3389/fonc.2021.631991.

6. Flies D.B., Langermann S., Jensen C., Karsdal M.A., Willumsen N. Regulation of tumor immunity and immunotherapy by the tumor collagen extracellular matrix. Front Immunol, 2023, vol.14, pp. 1199513. doi: 10.3389/fimmu.2023.1199513.

7. Larsen A.M.H., Kuczek D.E., Kalvisa A., Siersbæk M.S., Thorseth M.L., Johansen A.Z., Carretta M., Grøntved L., Vang O., Madsen D.H. Collagen density modulates the immunosuppressive functions of macrophages. J Immunol, 2020, vol. 205, pp. 1461–1472. doi: 10.4049/jimmunol.1900789.

8. Soles A., Selimovic A., Sbrocco K., Ghannoum F., Hamel K., Moncada E.L., Gilliat S., Cvetanovic M. Extracellular Matrix Regulation in Physiology and in Brain Disease. Int J Mol Sci, 2023, vol.8, pp. 7049. doi: 10.3390/ijms24087049.

9. Oudart J.B., Monboisse J.C., Maquart F.X., Brassart B., Brassart-Pasco S., Ramont L.. Type XIX collagen: A new partner in the interactions between tumor cells and their microenvironment. Matrix Biol, 2017, vol. 57-58, pp. 169-177. doi: 10.1016/j.matbio.2016.07.010.

10. Mammoto T., Jiang A., Jiang E., Panigrahy D., Kieran M.W., Mammoto A. Role of collagen matrix in tumor angiogenesis and glioblastoma multiforme progression. Am J Pathol, 2013, vol. 183, pp. 1293-1305. doi: 10.1016/j.ajpath.2013.06.026.

11. Tsai H.F., Chang Y.C., Li C.H. et al. Type V collagen alpha 1 chain promotes the malignancy of glioblastoma through PPRC1-ESM1 axis activation and extracellular matrix remodeling. Cell Death Discov, 2021, vol. 7, pp. 313. doi: 10.1038/s41420-021-00661-3.

12. Senner V., Ratzinger S., Mertsch S., Grässel S., Paulus W. Collagen XVI expression is upregulated in glioblastomas and promotes tumor cell adhesion. FEBS Lett, 2008, vol. 582, pp. 3293-3300. doi: 10.1016/j.febslet.2008.09.017.

13. Das A., Tan W.-L., Smith D.R. Expression of extracellular matrix markers in benign meningiomas. Neuropathology, 2003, vol. 23, pp. 275–281.

14. Nguyen T.T., Gobinet C., Feru J., Brassart-Pasco S., Manfait M., Piot O. Characterization of Type I and IV Collagens by Raman Microspectroscopy: Identification of Spectral Markers of the Dermo-Epidermal Junction. Spectroscopy: An International Journal, 2012, vol. 27, pp. 421–427. doi: 10.1155/2012/686183.

15. Haka A.S., Shafer-Peltier K. E., Fitzmaurice M., Crowe J., Dasari R.R., Feld M.S. Diagnosing breast cancer by using Raman spectroscopy Proceedings of the National Academy of Sciences of the United States of America, 2005, vol. 102, pp. 12371–12376. doi: 10.1073/pnas.0501390102.

16. D’Acunto M., Gaeta R., Capanna R. et al. Contribution of Raman Spectroscopy to Diagnosis and Grading of Chondrogenic Tumors. Scientific Reports, 2020, vol. 10,- pp. 2155. doi: 10.1038/s41598-020-58848-0.

17. Ingle I., Kerns J.G., Shepherd R.F. Multivariate analysis of Raman spectra for discriminating human collagens: In vitro identification of extracellular matrix collagens produced by an osteosarcoma cell line. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2025, vol. 328, pp. 125434. doi: 10.1016/j.saa.2024.125434.

18. Romanishkin I.D., Savelieva T.A., Ospanov A., Linkov K.G., Shugai S.V., Goryajnov S.A., Pavlova G.V., Pronin I.N., Loschenov V.B. Classification of intracranial tumors based on optical-spectral analysis. Biomedical Photonics, 2023, vol.12, pp. 4-10. doi: 10.24931/2413-9432-2023-12-3-4-10.

19. Ospanov A., Romanishkin I.D., Savelieva T.A., Shugay S.V., Kosyrkova A.V., Pavlova G.V., Pronin I.N., Loschenov V.B. Search for correlations in raman, diffuse reflectance, and fluorescence spectroscopy data from intracranial tumors. Biomedical Photonics, 2025, vol.14, pp. 22-33. doi: 10.24931/2413-9432-2025-14-4-22-33.

20. Brusatori M., Auner G., Noh T., et al. Intraoperative Raman Spectroscopy. Neurosurg Clin N Am, 2017, vol. 28, pp. 633-652. doi: 10.1016/j.nec.2017.05.014.


Review

For citations:


Antipova E.D., Romanishkin I.D., Savelieva T.A., Ryabova A.V., Shugay S.V., Kosyrkova A.V., Pavlova G.V., Pronin I.N., Loschenov V.B. Analysis of collagen presence in brain tumors using spontaneous Raman scattering spectroscopy. Biomedical Photonics. 2026;15(3):21-29. (In Russ.) https://doi.org/10.24931/2413-9432-2026-15-3-21-29

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