Comparative Viability Analysis of Monolayer Cell Suspension and Multicellular Tumor Spheroids as an In-vitro Tumor Model

Authors

  • Aziz Ur Rahman Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), Pakistan.
  • Zahoor Islam Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), Pakistan.
  • Abid Ullah Department of Pharmacy, Shaheed Benazir Bhutto University (SBBU) Sheringal Dir Upper, KP, Pakistan.
  • Muhammad Irfan Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), Pakistan.
  • Saeed Ahmad Department of Pharmacy, University of Malakand, Chakdara, Dir (Lower), Pakistan.
  • Sheikh Abdur Rashid Gomal Center of Pharmaceutical Sciences, Faculty of Pharmacy, Gomal University, Dera Ismail Khan, Pakistan.

DOI:

https://doi.org/10.70749/ijbr.v3i3.924

Keywords:

Monolayer Cell Culture, Multicellular Tumor Spheroids, Disaggregated Spheroids

Abstract

Background: Monolayer cell suspension has been used as an in-vitro model for investigating cells characteristics, drug penetration, and tissue research. 3-D multicellular tumor spheroids (3-D MCTS) have attained focus of researchers from the last three decades as a more valuable tool to study tumor biology. The superiority of MCTS has been elucidated here along with the effect of disaggregated spheroids. Method: The cellular differentiating fluorophores; calcein-AM and Propidium Iodide (PI) have been exploited for cells viability characteristics, where calcein-AM penetrate viable proliferating cells only, PI penetrate dead cells only, while viable hypoxic cell remains unstained and are resistant to penetration of either fluorophore. Fluorophores uptake in 3, 5, and 7-day old intact spheroids, disaggregated spheroids, and monolayer cell suspension has been investigated. Results: The Calcein-AM stained cells and unstained cells fraction in intact, disaggregated, and monolayer cell suspension was statistically non-significant (ANOVA p = 0.072 and 0.411 respectively), while the PI-stained cells fraction showed statistical significance (ANOVA, p = 0.012). PI-stained cells fraction was greater in intact spheroids followed by disaggregated spheroids with a minimum fraction in monolayer cell suspension. This effect could be due to compact nature, microenvironment, and deficient drainage in spheroids mimicking in-vivo tumor.  Conclusion: The disaggregated spheroids serve as intermediate between intact spheroids and monolayer cell suspension. The intact spheroids possess superiority over monolayer cell suspension being more compact, and resemblance to in-vivo tumors to elucidate tumor biology.

Downloads

Download data is not yet available.

References

Foglietta, F., et al., Methodological aspects and pharmacological applications of three-dimensional cancer cell cultures and organoids. Life Sciences, 2020. 254: p. 117784. https://doi.org/10.1016/j.lfs.2020.117784

Argenziano, M., et al., Biological effect evaluation of glutathione-responsive cyclodextrin-based nanosponges: 2D and 3D studies. Molecules, 2020. 25(12): p. 2775. https://doi.org/10.3390/molecules25122775

Han, S.J., S. Kwon, and K.S. Kim, Challenges of applying multicellular tumor spheroids in preclinical phase. Cancer cell international, 2021. 21: p. 1-19. https://doi.org/10.1186/s12935-021-01853-8

Dalir Abdolahinia, E. and X. Han, The three-dimensional in vitro cell culture models in the study of oral cancer immune microenvironment. Cancers, 2023. 15(17): p. 4266. https://doi.org/10.3390/cancers15174266

Rahman, A.U., et al., Multicellular Tumor Spheroids: A Comprehensive Review of Tumor Biology and Drug Delivery Strategies. Indus Journal of Bioscience Research, 2025. 3(1): p. 487-493. https://doi.org/10.70749/ijbr.v3i1.480

Nunes, A.S., et al., 3D tumor spheroids as in vitro models to mimic in vivo human solid tumors resistance to therapeutic drugs. Biotechnology and bioengineering, 2019. 116(1): p. 206-226. https://doi.org/10.1002/bit.26845

Fernandes, S., et al., Tumor in 3D: in vitro complex cellular models to improve nanodrugs cancer therapy. Current medicinal chemistry, 2020. 27(42): p. 7234-7255. https://doi.org/10.2174/0929867327666200625151134

Mueller-Klieser, W., J. Freyer, and R. Sutherland, Influence of glucose and oxygen supply conditions on the oxygenation of multicellular spheroids. British journal of cancer, 1986. 53(3): p. 345-353. https://doi.org/10.1038/bjc.1986.58

Casciari, J.J., S.V. Sotirchos, and R.M. Sutherland, Glucose diffusivity in multicellular tumor spheroids. Cancer research, 1988. 48(14): p. 3905-3909.

Venkatasubramanian, R., M.A. Henson, and N.S. Forbes, Incorporating energy metabolism into a growth model of multicellular tumor spheroids. Journal of theoretical biology, 2006. 242(2): p. 440-453. https://doi.org/10.1016/j.jtbi.2006.03.011

Bustamante, D.J., et al., Biofabrication of spheroids fusion-based tumor models: computational simulation of glucose effects. Biofabrication, 2021. 13(3): p. 035010. https://doi.org/10.1088/1758-5090/abe025

Burleson, K.M., L.K. Hansen, and A.P.N. Skubitz, Ovarian carcinoma spheroids disaggregate on type I collagen and invade live human mesothelial cell monolayers. Clinical & Experimental Metastasis, 2005. 21(8): p. 685-697. https://doi.org/10.1007/s10585-004-5768-5

Yuhas, J.M., et al., A simplified method for production and growth of multicellular tumor spheroids. Cancer Res, 1977. 37(10): p. 3639-43.

Thoma, C.R., et al., 3D cell culture systems modeling tumor growth determinants in cancer target discovery. Adv Drug Deliv Rev, 2014. 69-70: p. 29-41. https://doi.org/10.1016/j.addr.2014.03.001

Rahman, A.U., et al., Exploring Hiv-1 Tat Penetrability in Tumor Spheroids Through Confocal Microscopy: a Cell Lines Based Study. The Journal of Population Therapeutics and Clinical Pharmacology, 2024. 31(8): p. 2682-2693. https://doi.org/10.53555/2bky4n93

Ur Rahman, A., S. Khan, and M. Khan, Transport of trans-activator of transcription (TAT) peptide in tumour tissue model: evaluation of factors affecting the transport of TAT evidenced by flow cytometry. Journal of Pharmacy and Pharmacology, 2020. 72(4): p. 519-530. https://doi.org/10.1111/jphp.13221

Dwarkanath, B. and V. Jain, Energy linked modifications of the radiation response in a human cerebral glioma cell line. International Journal of Radiation Oncology* Biology* Physics, 1989. 17(5): p. 1033-1040. https://doi.org/10.1016/0360-3016(89)90152-1

Jain, V., et al., Effects of 2-deoxy-D-glucose on glycolysis, proliferation kinetics and radiation response of human cancer cells. International Journal of Radiation Oncology* Biology* Physics, 1985. 11(5): p. 943-950. https://doi.org/10.1016/0360-3016(85)90117-8

Dwarkanath, B., Energy metabolism and repair of radiation induced damage in brain tumors. National Institute of Mental Health and Neurosciences Bangalore India, 1988.

Aziz-Ur-Rahman, et al., The cost-efficient techniques to evaluate the age-based structural heterogeneity and morphological analysis of multicellular tumor spheroids. Pakistan Journal of Pharmaceutical Sciences, 2025. 38(1): p. 129-137.

Carlsson, j., et al., Formation and Growth of Multicellular Spheroids of Human Origin. Int. J. Cancer 1983. 31: p. 523-533. https://doi.org/10.1002/ijc.2910310502

Martin, M. and T. Risler, Viscocapillary instability in cellular spheroids. New journal of physics, 2021. 23(3): p. 033032. https://doi.org/10.1088/1367-2630/abe9d6

Vinci, M., et al., Advances in establishment and analysis of three-dimensional tumor spheroid-based functional assays for target validation and drug evaluation. BMC Biology, 2012. 10(1): p. 29. https://doi.org/10.1186/1741-7007-10-29

Minchinton, A.I. and I.F. Tannock, Drug penetration in solid tumours. Nat Rev Cancer, 2006. 6(8): p. 583-592. https://doi.org/10.1038/nrc1893

Downloads

Published

2025-03-31

How to Cite

Aziz Ur Rahman, Islam, Z., Abid Ullah, Irfan, M., Ahmad, S., & Rashid, S. A. (2025). Comparative Viability Analysis of Monolayer Cell Suspension and Multicellular Tumor Spheroids as an In-vitro Tumor Model. Indus Journal of Bioscience Research, 3(3), 613-618. https://doi.org/10.70749/ijbr.v3i3.924