Generic placeholder image

Current Drug Therapy

Editor-in-Chief

ISSN (Print): 1574-8855
ISSN (Online): 2212-3903

Mini-Review Article

Miscellaneous Naturally Derived Anticancer Agents

Author(s): Saranya Punniyakotti, Rashmi Saxena Pal*, Kanav Khera and Deepti Katiyar

Volume 18, Issue 5, 2023

Published on: 05 May, 2023

Page: [357 - 364] Pages: 8

DOI: 10.2174/1574885518666230330162748

Price: $65

conference banner
Abstract

Secondary metabolites of natural origin exhibit numerous pharmacological activities, like anti-inflammatory and anti-oxidant effects. Lipid peroxidation has been observed to be prevented by terminating free radical chains and chelating redox active metal ions. These properties of the secondary products can also aid in preventing carcinoma. Many traditional and emerging plants are blessed with plenty of unexplored phytometabolites, which contain the probability to carry huge antineoplastic potential. Acetogenins are anticancer compounds that kill tumor cells through a variety and series of developmental methods. They are very powerful apoptosis inducers that can regulate the exclusion of chemotherapy medicines from cancer cells. Chalcone is a pharmacologically active molecule that can be found in both natural and manufactured products. Marine species, which are also examples of naturally derived drug sources, such as algae, sponges, tunicates, and bryozoans, have emerged as important components of choice for the separation of novel anticancer drugs obtained from marine sources. Bacteria of marine origin are the source of new drug discoveries and therapeutic targets, which are being explored to unprecedented heights, and they have proven to be sources of various medicinal agents, such as antibiotics, etc. Numerous secondary metabolites have been isolated from marine fungi that were active biologically, structurally unique, and also therapeutically beneficial. So far, almost 1000 secondary metabolites have been found, the majority of which are exclusive to lichens. This mini-review discusses different aspects related to the natural derivatives obtained from various sources, which play a pivotal role as anti-neoplastic agents.

Next »
Graphical Abstract

[1]
Garg MP. Darokar v, Sundaresan U, Faridi SR, Luqman S, Khanuja S. Anticancer activity of some medicinal plants from high altitude evergreen elements of Indian Western Ghats. J Res Educ Indian Med 2007; XIII(3): 1-6.
[2]
Kumar S, Suresh PK, Vijaybabu MR, Arunkumar A, Arunakaran J. Anticancer effects of ethanolic neem leaf extract on prostate cancer cell line (PC-3). J Ethnopharmacol 2006; 105(1-2): 246-50.
[3]
Ochwang’i DO, Kimwele CN, Oduma JA, Gathumbi PK, Mbaria JM, Kiama SG. Medicinal plants used in treatment and management of cancer in Kakamega County, Kenya. J Ethnopharmacol 2014; 151(3): 1040-55.
[http://dx.doi.org/10.1016/j.jep.2013.11.051] [PMID: 24362078]
[4]
Mangal M, Sagar P, Singh H, Raghava GPS, Agarwal SM. NPACT: Naturally occurring plant-based anti-cancer compound-activity target database. Nucleic Acids Res 2013; 41(D1): D1124-9.
[http://dx.doi.org/10.1093/nar/gks1047] [PMID: 23203877]
[5]
Jha R, Zi-rong X. Biomedical compounds from marine organisms. Mar Drugs 2004; 2(3): 123-46.
[http://dx.doi.org/10.3390/md203123]
[6]
Aggarwal BB, Kumar A, Bharti AC. Anticancer potential of curcumin: preclinical and clinical studies. Anticancer Res 2003; 23(1A): 363-98.
[PMID: 12680238]
[7]
Costa M, Garcia M, Costa-Rodrigues J, et al. Exploring bioactive properties of marine cyanobacteria isolated from the Portuguese coast: High potential as a source of anticancer compounds. Mar Drugs 2013; 12(1): 98-114.
[http://dx.doi.org/10.3390/md12010098] [PMID: 24384871]
[8]
Lavakumar V, Ahamed K, Ravichandran V. Anticancer and antioxidant effect of Acanthophora spicifera against EAC induced carcinoma in mice. J Pharm Res 2012; 5: 1503-7.
[9]
Manilal A, Sujith S, Kiran GS, et al. Biopotentials of seaweeds collected from the southwest coast of India. J Mar Sci Technol 2009; 17: 67-73.
[10]
Prakash O, Kumar A, Kumar P. Anticancer potential of plants and natural products. American J Phcological Sci 2013; 1(6): 104-15.
[11]
Wamidh HT. Anticancer and Antimicrobial Potential of Plant-Derived Natural Products. In: Phytochemicals-Bioactivities and Impact on Health. 2011; pp. 142-58.
[12]
Merina N, Chandra KJ, Kotoky J. Medicinal plants with potential anticancer activity: Review A. Int Res J Pharm 2012; 3(6): 26-30.
[13]
Z., Michael S., Eran Ben-A., and Bashar S., Greco-Arab and Islamic Herbal-Derived Anticancer Modalities: From Tradition to Molecular Mechanisms. Evid Based Complement Alternat Med 2012; 13.
[14]
Sharma H, Parihar L, Parihar P. Review on anticancerous properties of some medicinal plants. J Med Plants Res 2011; 5(10): 1818-35.
[15]
Solowey E, Lichtenstein M, Sallo S, Paavilainen H, Solowet E. Lorberboum- Galski H. Evaluating medicinal plants for anticancer activity. ScientificWorldJournal 2014; 721402: 12.
[16]
Shoeb M. Anti-cancer agents from medicinal plants. Bang J Pharmacol 2006; 1(2): 35-41.
[17]
El-Bondkly EAM, El-Bondkly AAM, El-Bondkly AAM. Marine endophytic fungal metabolites: A whole new world of pharmaceutical therapy exploration. Heliyon 2021; 7(3): e06362.
[http://dx.doi.org/10.1016/j.heliyon.2021.e06362] [PMID: 33869822]
[18]
Sandrawati N, Hati SP, Yunita F, et al. Antimicrobial and cytotoxic activities of marine sponge-derived fungal extracts isolated from Dactylospongia sp. J Appl Pharm Sci 2020; 10(4): 28-33.
[http://dx.doi.org/10.7324/JAPS.2020.104005]
[19]
Tallei TE. Antimicrobial activity screening of endophytic fungi extracts isolated from brown algae Padina sp. J Appl Pharm Sci 2019; 9(3): 9-13.
[http://dx.doi.org/10.7324/JAPS.2019.90302]
[20]
Weerakoon G, Wolseley P, Will-Wolf S, Wijeyaratne C. Corticolous lichen species as indicators of disturbed/undisturbed vegetation types in the central mountains of Sri Lanka. Lichenol 2020; 52(3): 233-45.
[http://dx.doi.org/10.1017/S0024282920000109]
[21]
Machida K, Tanaka T, Fujita K, Taniguchi M. Farnesol-induced generation of reactive oxygen species via indirect inhibition of the mitochondrial electron transport chain in the yeast Saccharomyces cerevisiae. J Bacteriol 1998; 180(17): 4460-5.
[http://dx.doi.org/10.1128/JB.180.17.4460-4465.1998] [PMID: 9721283]
[22]
Bostedor RG, Karkas JD, Arison BH, et al. Farnesol-derived dicarboxylic acids in the urine of animals treated with zaragozic acid A or with farnesol. J Biol Chem 1997; 272(14): 9197-203.
[http://dx.doi.org/10.1074/jbc.272.14.9197] [PMID: 9083051]
[23]
Greenwell M, Rahman PK. Medicinal plants: Their use in anticancer treatment. Int J Pharm Sci Res 2015; 6(10): 4103-12.
[PMID: 26594645]
[24]
Desai A, Qazi G, Ganju R, et al. Medicinal plants and cancer chemoprevention. Curr Drug Metab 2008; 9(7): 581-91.
[http://dx.doi.org/10.2174/138920008785821657] [PMID: 18781909]
[25]
Juyal D, Thawani V, Thaledi S, Joshi M. Ethnomedical properties of taxus wallichiana zucc. (Himalayan yew). J Tradit Complement Med 2014; 4(3): 159-61.
[http://dx.doi.org/10.4103/2225-4110.136544] [PMID: 25161920]
[26]
Kampan NC, Madondo MT, McNally OM, Quinn M, Plebanski M. Paclitaxel and its evolving role in the management of ovarian cancer. BioMed Res Int 2015; 2015: 1-21.
[http://dx.doi.org/10.1155/2015/413076] [PMID: 26137480]
[27]
Venditto VJ, Simanek EE. Cancer therapies utilizing the camptothecins: A review of the in vivo literature. Mol Pharm 2010; 7(2): 307-49.
[http://dx.doi.org/10.1021/mp900243b] [PMID: 20108971]
[28]
Guadagnolo BA, Petereit DG, Coleman CN. Cancer care access and outcomes for American Indian populations in the united states: Challenges and models for progress. Semin Radiat Oncol 2017; 27(2): 143-9.
[http://dx.doi.org/10.1016/j.semradonc.2016.11.006] [PMID: 28325240]
[29]
Lichota A, Gwozdzinski K. Anticancer activity of natural compounds from plant and marine environment. Int J Mol Sci 2018; 19(11): 3533.
[http://dx.doi.org/10.3390/ijms19113533] [PMID: 30423952]
[30]
Kirdeeva Y, Fedorova O, Daks A, Barlev N, Shuvalov O. How should the worldwide knowledge of traditional cancer healing be integrated with herbs and mushrooms into modern molecular pharmacology? Pharmaceuticals (Basel) 2022; 15(7): 868.
[http://dx.doi.org/10.3390/ph15070868] [PMID: 35890166]
[31]
Karatoprak GŞ, Küpeli Akkol E, Genç Y, Bardakci H, Yücel Ç, Sobarzo-Sánchez E. Combretastatins: An overview of structure, probable mechanisms of action and potential applications Molecules 2020; 25(11): 2560.
[32]
Chavda VP, Patel AB, Mistry KJ, et al. Nano-Drug delivery systems entrapping natural bioactive compounds for cancer: Recent progress and future challenges. Front Oncol 2022; 12: 867655.
[http://dx.doi.org/10.3389/fonc.2022.867655] [PMID: 35425710]
[33]
Long S, Resende DISP, Kijjoa A, et al. Antitumor activity of Quinazolinone Alkaloids inspired by marine natural products. Mar Drugs 2018; 16(8): 261.
[http://dx.doi.org/10.3390/md16080261] [PMID: 30065225]
[34]
Mujeeb F, Bajpai P, Pathak N. Phytochemical evaluation, antimicrobial activity, and determination of bioactive components from leaves of Aegle marmelos. BioMed Res Int 2014; 2014: 1-11.
[http://dx.doi.org/10.1155/2014/497606] [PMID: 24900969]
[35]
Radha MH, Laxmipriya NP. Evaluation of biological properties and clinical effectiveness of Aloe vera: A systematic review. J Tradit Complement Med 2015; 5(1): 21-6.
[http://dx.doi.org/10.1016/j.jtcme.2014.10.006] [PMID: 26151005]
[36]
Sánchez M, González-Burgos E, Iglesias I, Gómez-Serranillos MP. Pharmacological update properties of Aloe Vera and its major active constituents. Molecules 2020; 25(6): 1324.
[http://dx.doi.org/10.3390/molecules25061324] [PMID: 32183224]
[37]
Iyare GI, Omorodion NT, Erameh TO, et al. The effects of Anacardium occidentale leave extract on histology of selected organs of Wistar rats. MOJ Biol Med 2017; 2(2): 216-21.
[38]
Li X, Qu L, Dong Y, et al. A review of recent research progress on the astragalus genus. Molecules 2014; 19(11): 18850-80.
[http://dx.doi.org/10.3390/molecules191118850] [PMID: 25407722]
[39]
Ahmad N, Feyes DK, Agarwal R, Mukhtar H, Nieminen A-L. Green tea constituent epigallocatechin-3-gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells. J Natl Cancer Inst 1997; 89(24): 1881-6.
[http://dx.doi.org/10.1093/jnci/89.24.1881] [PMID: 9414176]
[40]
Ohiagu FO, Chikezie PC, Chikezie CM, Enyoh CE. Anticancer activity of Nigerian medicinal plants: A review. Fut J Pharm Sci 2021; 7(1): 70.
[http://dx.doi.org/10.1186/s43094-021-00222-6]
[41]
Lee WYW, Cheung CCM, Liu KWK, et al. Cytotoxic effects of tanshinones from Salvia miltiorrhiza on doxorubicin-resistant human liver cancer cells. J Nat Prod 2010; 73(5): 854-9.
[http://dx.doi.org/10.1021/np900792p] [PMID: 20455578]
[42]
Yoon Y, Kim YO, Jeon WK, Park HJ, Sung HJ. Tanshinone IIA isolated from Salvia miltiorrhiza BUNGE induced apoptosis in HL60 human premyelocytic leukemia cell line. J Ethnopharmacol 1999; 68(1-3): 121-7.
[http://dx.doi.org/10.1016/S0378-8741(99)00059-8] [PMID: 10624871]
[43]
Bian W, Chen F, Bai L, Zhang P, Qin W. Dihydrotanshinone I inhibits angiogenesis both in vitro and in vivo. Acta Biochim Biophys Sin (Shanghai) 2008; 40(1): 1-6.
[http://dx.doi.org/10.1111/j.1745-7270.2008.00370.x] [PMID: 18180848]
[44]
Alabsi AM, Ali R, Ali AM, et al. Induction of caspase-9, biochemical assessment and morphological changes caused by apoptosis in cancer cells treated with goniothalamin extracted from Goniothalamus macrophyllus. Asian Pac J Cancer Prev 2013; 14(11): 6273-80.
[http://dx.doi.org/10.7314/APJCP.2013.14.11.6273] [PMID: 24377517]
[45]
Salehi B, Fokou PVT, Yamthe LRT, et al. Phytochemicals in prostate cancer: From bioactive molecules to upcoming therapeutic agents. Nutrients 2019; 11(7): 1483.
[http://dx.doi.org/10.3390/nu11071483] [PMID: 31261861]
[46]
Olsson M, Zhivotovsky B. Caspases and cancer. Cell Death Differ 2011; 18(9): 1441-9.
[http://dx.doi.org/10.1038/cdd.2011.30] [PMID: 21455218]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy