Preliminary data on cytotoxicity and functional group assessment of a herb–mineral combination against colorectal carcinoma cell line
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Remya Jayakumar
, Saumya Gulati
Abstract
Objectives
The invasive screening methods and the late stage diagnosis of colorectal carcinoma (CRC) are contributing for the devastative prognosis. The gradual shift of the disease pattern among younger generations requires the implementation of phytochemicals and traditional medicines. Arkeshwara rasa (AR) is a herb–mineral combination of Tamra bhasma/incinerated copper ashes and Dwigun Kajjali/mercury sulphide levigated with Calotropis procera leaf juice, Plumbago zeylanica root decoction and the decoction of three myrobalans (Terminalia chebula, Terminalia bellerica, Emblica Officinalis decoction)/Triphala decoction.
Methods
The SW-480 cell line was checked for the cytotoxicity and the cell viability criteria with MTT(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide) assay. The acridine orange/ethidium bromide (AO/EtBr) assay revealed the depth of apoptosis affected cells in the fluorescent images. The FTIR analysis exhibited the graphical spectrum of functional groups within the compound AR.
Results
The IC50 from the 10−7 to 10−3 concentrations against SW-480 cells was 40.4 μg/mL. The staining of AO/EtBr was performed to visualize live and dead cells and it is evident from the result that number of apoptotic cells increases at increasing concentration of AR. The single bond with stretch vibrations of O–H and N–H are more concentrated in the 2,500–3,200 cm−1 and 3,700–4,000 cm−1 of the spectra whereas, the finger print region carries the O–H and S=O type peaks.
Conclusions
The AR shows strong cyto-toxicity against the SW-480 cells by inducing apoptosis. It also modulates cellular metabolism with the involvement of functional groups which antagonizes the strong acids. Moreover, these effects need to be analyzed further based in the in vivo and various in vitro models.
Acknowledgments
If applicable.
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Research ethics: The local Institutional Review Board deemed the study exempt from review.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Research funding: None declared.
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Data availability: Not applicable.
References
1. Nishiumi, S, Kobayashi, T, Kawana, S, Unno, Y. Investigations in the possibility of early detection of colorectal cancer by gas chromatography/triple-quadrupole mass spectrometry. 2017.10.18632/oncotarget.15081Search in Google Scholar PubMed PubMed Central
2. Rawla, P, Sunkara, T, Barsouk, A. Epidemiology of colorectal cancer: incidence, mortality, survival, and risk factors. Prz Gastroenterol 2019;14:89–103. https://doi.org/10.5114/pg.2018.81072.Search in Google Scholar PubMed PubMed Central
3. Xi, Y, Xu, P. Translational oncology global colorectal cancer burden in 2020 and projections to 2040. Transl Oncol 2021;14:101174. https://doi.org/10.1016/j.tranon.2021.101174.Search in Google Scholar PubMed PubMed Central
4. Institute NC. Cancer stat facts: colorectal cancer [Internet]. Available from: https://seer.cancer.gov/statfacts/html/colorect.html#content.Search in Google Scholar
5. Institute NC. Why is colorectal cancer rising rapidly among young adults? [Internet]. NCI. 1 p. Available from: https://www.cancer.gov/news-events/cancer-currents-blog/2020/colorectal-cancer-rising-younger-adults.Search in Google Scholar
6. Khoo, AM-G, Lau, J, Loh, X-S, Ng, CW-T, Griva, K, Tan, K-K. Understanding the psychosocial impact of colorectal cancer on young-onset patients: a scoping review. Cancer Med 2022;11:1688–700. https://doi.org/10.1002/cam4.4575.Search in Google Scholar PubMed PubMed Central
7. Qaderi, SM, Galjart, B, Verhoef, C, Slooter, GD, Koopman, M, Verhoeven, RHA, et al.. Disease recurrence after colorectal cancer surgery in the modern era: a population-based study. Int J Colorectal Dis 2021;36:2399–410. https://doi.org/10.1007/s00384-021-03914-w.Search in Google Scholar PubMed PubMed Central
8. Stengel, ST, Fazio, A, Lipinski, S, Jahn, MT, Aden, K, Ito, G, et al.. Activating transcription factor 6 mediates inflammatory signals in intestinal epithelial cells upon endoplasmic reticulum stress. Gastroenterology 2020;159:1357–74.e10.10.1053/j.gastro.2020.06.088Search in Google Scholar PubMed PubMed Central
9. Kaźmierczak-Siedlecka, K, Daca, A, Fic, M, van de Wetering, T, Folwarski, M, Makarewicz, W. Therapeutic methods of gut microbiota modification in colorectal cancer management – fecal microbiota transplantation, prebiotics, probiotics, and synbiotics. Gut Microb 2020;11:1518–30. https://doi.org/10.1080/19490976.2020.1764309.Search in Google Scholar PubMed PubMed Central
10. An, X, Bao, Q, Di, S, Zhao, Y, Zhao, S, Zhang, H, et al.. The interaction between the gut Microbiota and herbal medicines. Biomed Pharmacother 2019;118:109252. https://doi.org/10.1016/j.biopha.2019.109252.Search in Google Scholar PubMed
11. Barone, M, D’Amico, F, Brigidi, P, Turroni, S. Gut microbiome–micronutrient interaction: the key to controlling the bioavailability of minerals and vitamins? Biofactors 2022;48:307–14. https://doi.org/10.1002/biof.1835.Search in Google Scholar PubMed PubMed Central
12. Zhong, X, Di, Z, Xu, Y, Liang, Q, Feng, K, Zhang, Y, et al.. Mineral medicine: from traditional drugs to multifunctional delivery systems. Chin Med 2022;17:21. https://doi.org/10.1186/s13020-022-00577-9.Search in Google Scholar PubMed PubMed Central
13. Shin, SA, Joo, BJ, Lee, JS, Ryu, G, Han, M, Kim, WY, et al.. Phytochemicals as anti-inflammatory agents in animal models of prevalent inflammatory diseases. Molecules 2020;25:1–27. https://doi.org/10.3390/molecules25245932.Search in Google Scholar PubMed PubMed Central
14. Zhang, H, Yi, G. Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells. Onco Targets Ther 2019;12:4047–54. https://doi.org/10.2147/OTT.S200873.Search in Google Scholar PubMed PubMed Central
15. Eldhose, B, Gunawan, M, Rahman, M, Latha, MS, Notario, V. Plumbagin reduces human colon cancer cell survival by inducing cell cycle arrest and mitochondria-mediated apoptosis. Int J Oncol 2014;45:1913–20. https://doi.org/10.3892/ijo.2014.2592.Search in Google Scholar PubMed PubMed Central
16. Vadde, R, Radhakrishnan, S, Reddivari, L, Vanamala, JKP. Triphala extract suppresses proliferation and induces apoptosis in human colon cancer stem cells via suppressing c-Myc/Cyclin D1 and elevation of Bax/Bcl-2 ratio. Biomed Res Int 2015;2015:1–12. https://doi.org/10.1155/2015/649263.Search in Google Scholar PubMed PubMed Central
17. Wang, M, Li, Y, Hu, X. Chebulinic acid derived from triphala is a promising antitumour agent in human colorectal carcinoma cell lines. 2018;5:1–9, https://doi.org/10.1186/s12906-018-2412-5.Search in Google Scholar PubMed PubMed Central
18. Ghasemi, P, Shafiee, G, Ziamajidi, N, Abbasalipourkabir, R. Copper nanoparticles induce apoptosis and oxidative stress in SW480 human colon cancer cell line. Biol Trace Elem Res 2023;201:3746–54. https://doi.org/10.1007/s12011-022-03458-2.Search in Google Scholar PubMed
19. Dash, MK, Joshi, N, Dubey, VS, Dwivedi, KN, Gautam, DNS. Screening of anti-cancerous potential of classical Raudra rasa and modified Raudra rasa modified with hiraka bhasma (nanodiamond) through FTIR & LC-MS analysis. J Complement Integr Med 2022;19:669–82. https://doi.org/10.1515/jcim-2021-0410.Search in Google Scholar PubMed
20. Pranacharya Sri Sadananda Sharma PKS. Rasa Tarangini. Taranga: Motilal Banarasidas; 2014, vol 5:27–9 pp.Search in Google Scholar
21. Kulkarni, DA. Rasaratna Samuchaya, 2017th ed. Adhyaya: Meharchand Lakshman Das; 2017, ch 5:13:93 p.Search in Google Scholar
22. Kulkarni, DA. Rasaratna Samuchaya, 2017th ed. Adhyaya: Meharchand Lakshman Das; 2017, ch 5:52:101 p.Search in Google Scholar
23. Kulkarni, DA. Rasaratna Samuchaya, 2017th ed. Adhyaya: Meharchand Lakshman Das; 2017, ch 5:53:101 p.Search in Google Scholar
24. Pranacharya Sri Sadananda Sharma PKS. Rasa Tarangini. 2014th ed. Taranga: Motilal Banarasidas; 2014, vol 17:37–8 pp.Search in Google Scholar
25. Riss, TL, Moravec, RA, Niles, AL, Benink, HA, Worzella, TJ, Minor, L. Cell viability assays. Eli Lilly & Company and the National Center for Advancing Translational Sciences Bethesda (MD); 2016:1–25 pp. Available from: https://www.ncbi.nlm.nih.gov/books/NBK144065/. 23805433.Search in Google Scholar PubMed
26. Byvaltsev, VA, Bardonova, LA, Onaka, NR, Polkin, RA, Ochkal, SV, Shepelev, VV, et al.. Acridine orange: a review of novel applications for surgical cancer imaging and therapy. Front Oncol 2019;9:925. https://doi.org/10.3389/fonc.2019.00925.Search in Google Scholar PubMed PubMed Central
27. Winitchaikul, T, Sawong, S, Surangkul, D, Srikummool, M, Somran, J, Pekthong, D, et al.. Calotropis gigantea stem bark extract induced apoptosis related to ROS and ATP production in colon cancer cells. PLoS One 2021;16:e0254392. https://doi.org/10.1371/journal.pone.0254392.Search in Google Scholar PubMed PubMed Central
28. Nikbakht, H, Hassanipour, S, Shojaie, L, Vali, M, Ghaffari-fam, S, Ghelichi-ghojogh, M, et al.. Survival rate of colorectal cancer in Eastern Mediterranean region countries: a systematic review and meta-analysis. 2020;27:1–15, https://doi.org/10.1177/1073274820964146.Search in Google Scholar PubMed PubMed Central
29. Yuan, Y, Li, M, Hu, H, Dong, C, Chen, J, Li, X, et al.. Prognostic and survival analysis of 837 Chinese colorectal cancer patients. World J Gastroenterol 2013;19:2650–9. https://doi.org/10.3748/wjg.v19.i17.2650.Search in Google Scholar PubMed PubMed Central
30. Coleman, MP, Forman, D, Bryant, H, Butler, J, Rachet, B, Maringe, C, et al.. Cancer survival in Australia, Canada, Denmark, Norway, Sweden, and the UK, 1995–2007 (the International Cancer Benchmarking Partnership): an analysis of population-based cancer registry data. Lancet 2011;377:127–38. https://doi.org/10.1016/s0140-6736(10)62231-3.Search in Google Scholar PubMed PubMed Central
31. Thokanit, NS, Promchana, S, Thonkamdee, T, Jitkasikorn, P, Siripoon, T, Ngamphaiboon, N, et al.. Clinical study of long-term survival in colorectal cancer patients in Thailand: a 10-year follow-up. Iran J Public Health 2022;51:2538–48. https://doi.org/10.18502/ijph.v51i11.11171.Search in Google Scholar PubMed PubMed Central
32. Kim, SH, Lim, YJ. The role of microbiome in colorectal carcinogenesis and its clinical potential as a target for cancer treatment. Intest Res 2022;20:31–42. https://doi.org/10.5217/ir.2021.00034.Search in Google Scholar PubMed PubMed Central
33. Cheng, Y, Ling, Z, Li, L. The intestinal microbiota and colorectal cancer. 2020;11:1–13, https://doi.org/10.3389/fimmu.2020.615056.Search in Google Scholar PubMed PubMed Central
34. Zeller, G, Tap, J, Voigt, AY, Sunagawa, S, Kultima, JR, Paul, I, et al.. Potential of fecal microbiota for early-stage detection of colorectal cancer. Mol Syst Biol 2014;10:766. https://doi.org/10.15252/msb.20145645.Search in Google Scholar PubMed PubMed Central
35. Mitra, AK, Agrahari, V, Mandal, A, Cholkar, K, Natarajan, C, Shah, S, et al.. Novel delivery approaches for cancer therapeutics. J Control Release 2015;219:248–68. https://doi.org/10.1016/j.jconrel.2015.09.06.Search in Google Scholar
36. Yan, J, Zhan, X, Zhang, Z, Chen, K, Wang, M, Sun, Y, et al.. Tetrahedral DNA nanostructures for effective treatment of cancer: advances and prospects. J Nanobiotechnology 2021;19:412. https://doi.org/10.1186/s12951-021-01164-0.Search in Google Scholar PubMed PubMed Central
37. Joshi, N, Dash, MK, Dwivedi, L, Khilnani, GD. Toxicity study of Lauha Bhasma (calcined iron) in albino rats. Anc Sci Life 2016;35:159–66. https://doi.org/10.4103/0257-7941.179870.Search in Google Scholar PubMed PubMed Central
38. Sharma, P, Madhyastha, H, Madhyastha, R, Nakajima, Y, Maruyama, M, Verma, KS, et al.. An appraisal of cuticular wax of Calotropis procera (Ait.) R. Br.: extraction, chemical composition, biosafety and application. J Hazard Mater 2019;368:397–403. https://doi.org/10.1016/j.jhazmat.2019.01.067.Search in Google Scholar PubMed
39. Amala, E, Jeyaraj, M. Determination of antibacterial, antifungal, bioactive constituents of triphala by FT-IR and GC-MS analysis. Int J Pharm Pharm Sci 2014;6:123–6.Search in Google Scholar
40. Choedon, T, Mathan, G, Arya, S, Kumar, VL, Kumar, V. Anticancer and cytotoxic properties of the latex of Calotropis procera in a transgenic mouse model of hepatocellular carcinoma. World J Gastroenterol 2006;12:2517–22. https://doi.org/10.3748/wjg.v12.i16.2517.Search in Google Scholar PubMed PubMed Central
41. Mohapatra, S, Mohanty, J, Pani, S, Hansdah, S, Biswal, AK, Sahoo, AK, et al.. Root extract of Plumbago zeylanica L. induces cytotoxicity, inhibits cell migration and induces S-phase cell cycle arrest through down regulation of EGFR in HeLa cervical cancer cells. Adv Cancer Biol – Metastasis 2022;4:100027. https://doi.org/10.1016/j.adcanc.2022.100027.Search in Google Scholar
42. Jayakumar, R, Joshi, N, Dash, MK. Dietary supplements and nutraceuticals in the management of endocrine Disorders, endocrinological challenges in aging and nutraceuticals. In: Taylor and Francis. USA: CRC Press; 2021:169–95 pp.10.1201/9781003110866-8Search in Google Scholar
43. Jayakuma, R, Dash, MK, Kuma, P, Sharma, S, Gulati, S, Pandey, A, et al.. Pharmaceutical characterization and in-vitro anti cancer activity of Arkeshwara rasa against MDA-MB-23 cell line. J Ayu Her Integr Med 2023;100823. file://s1hcifs01/DEMProfiles/19838/Downloads/Proof%20version.pdf.10.1016/j.jaim.2023.100823Search in Google Scholar
44. Wan, Y, Zhang, J, Li, X, Wang, Y, Liu, Q. Cellular states and secondary chemical bonding: a biochemical view of major human diseases. Biochem Insights 2019;12:1–2. https://doi.org/10.1177/1178626419877846.Search in Google Scholar PubMed PubMed Central
45. Dash, MK, Joshi, N, Gautam, DNS, Jayakumar, R, Tripathi, YB. Ayurvedic supportive therapy in the management of breast cancer. J Herb Med 2021;29:100490. https://doi.org/10.1016/j.hermed.2021.100490.Search in Google Scholar
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- Frontmatter
- Reviews
- Markhamia lutea leaves aqueous and ethanolic extract with curative anti-inflammatory activity attenuates paclitaxel toxicity in rat’s intestine
- Does hydrotherapy influence plasma glucose levels in type 2 diabetes? – A scoping review
- Comparative effectiveness is the common denominator in health services research: experimental effects are promising, real-world effects are compelling
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- Antipyretic activity of the hydro-alcoholic extract of Artemisia absinthium L. as a standalone and as an adjuvant with barley water against yeast-induced pyrexia in albino Wistar rats
- Selenium prevented renal tissue damage in lipopolysaccharide-treated rats
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