Research Article
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Year 2025, Volume: 29 Issue: 5, 1823 - 1834, 01.09.2025
https://doi.org/10.12991/jrespharm.1763436

Abstract

References

  • Baliga MS, Kurian PJ. Ixora coccinea Linn.: Traditional uses, phytochemistry and pharmacology. Chin J Integr Med. 2012; 18(1): 72-79. https://doi.org/10.1007/s11655-011-0881-3
  • Annapurna J, Amarnath PV, Amar Kumar D, Ramakrishna SV, Raghavan KV. Antimicrobial activity of Ixora coccinea leaves. Fitoterapia. 2003; 74(3): 291-293. https://doi.org/10.1016/s0367-326x(03)00037-6
  • Latha PG, Panikkar KR. Cytotoxic and antitumor principles from Ixora coccinea flowers. Cancer Lett. 1998; 130(1-2) :197-202. https://doi.org/10.1016/s0304-3835(98)00140-2
  • Ratnasooriya WD, Deraniyagala SA, Galhena G, Liyanage SS, Bathige SD, Jayakody JR. Anti-inflammatory activity of the aqueous leaf extract of Ixora coccinea. Pharm Biol. 2005;43(2):147-152. https://doi.org/10.1080/13880200590919483
  • Anantharaju PG, Gowda PC, Vimalambike MG, Madhunapantula SV. An overview on the role of dietary phenolics for the treatment of cancers. Nutr J. 2016; 15(1): 99. https://doi.org/10.1186/s12937-016-0217-2
  • Dontha S, Kamurthy H, Manthripragada B. Phytochemical and pharmacological profile of Ixora: A Review. Int J Pharm Sci Res. 2015; 6(2): 567-584. http://doi.org/10.13040/IJPSR.0975-8232.6(2).567-84
  • Lin JP, Yang JS, Lin JJ, Lai KC, Lu HF, Ma CY, Sai-Chuen Wu R, Wu KC, Chueh FS, Gibson Wood W, Chung JG. Rutin inhibits human leukemia tumor growth in a murine xenograft model in vivo. Environ Toxicol. 2012; 27(8): 480– 484. https://doi.org/10.1002/tox.20662
  • Alonso-Castro AJ, Domínguez F, García-Carrancá A. Rutin exerts antitumor effects on nude mice bearing SW480 tumor. Arch Med Res. 2013; 44(5): 346–351. https://doi.org/10.1016/j.arcmed.2013.06.002
  • Yoshida T, Konishi M, Horinaka M, Yasuda T, Goda AE, Taniguchi H, Yano K, Wakada M, Sakai T. Kaempferol sensitizes colon cancer cells to TRAIL-induced apoptosis. Biochem Biophys Res Commun. 2008; 375(1): 129-133. https://doi.org/10.1016/j.bbrc.2008.07.131
  • Davis JM, Murphy EA, Carmichael MD. Effects of the dietary flavonoid quercetin upon performance and health. Curr Sports Med Rep. 2009; 8(4): 206-213. https://doi.org/10.1249/JSR.0b013e3181ae8959
  • Wall ME, Wani MC. Camptothecin and taxol: from discovery to clinic. J Ethnopharmacol. 1996; (1-3): 239-254. https://doi.org/10.1016/0378-8741(95)01367-9
  • Isah T, Umar S. Influencing in vitro clonal propagation of Chonemorpha fragrans (moon) Alston by culture media strength, plant growth regulators, carbon source and photo periodic incubation. J For Res. 2018; 31: 27-43. https://doi.org/10.1007/s11676-018-0794-3
  • Saravanan P, Boopalan E. Occurrence of Camptothecin, an anticancer drug from Ixora coccinea Linn. Int J Appl Biol. 2011; 2(2): 30-34.
  • Kavitha P, Vasantha Kumar T, Rajasekharan PE, Abdul Kareem VK, Rao VK. Camptothecin and 9-methoxy Camptothecin, anti-cancer alkaloids in Nothapodytes nimmoniana from Western Ghats, India. J Med Aromat Plant Sci. 2010; 32(2): 129-132.
  • Ghoshal DS, Kharat SN, Godbole SA. Phytochemical and comparative assessment of bark and root extracts of Ixora barbata Roxb. ex. Sm. and Ixora coccinea L. using high-performance thin layer chromatography assay. Indian J Pharm Sci. 2022; 84(3): 604-616. https://doi.org/10.36468/pharmaceutical-sciences.956
  • Nair SC, Panikkar KR. Antitumor principles from Ixora javanica. Cancer Lett. 1990; 49(2): 121–126. https://doi.org/10.1016/0304-3835(90)90147-p
  • Nair SC, Panikkar B, Akamanchi KG, Panikkar KR. Inhibitory effects of Ixora javanica extract on skin chemical carcinogenesis in mice and its antitumor activity. Cancer Lett. 1991; 60(3): 253–258. https://doi.org/10.1016/0304- 3835(91)90121-w
  • Mohammed M M D, Ibrahim N A, Chen M, Zhai L. Rubiothiazepine a novel unusual cytotoxic alkaloid from Ixora undulata Roxb. leaves. Nat Prod Chem Res. 2014; 2: 128. https://doi.org/10.4172/2329-6836.100012
  • Mohammed MMD, Mohamed KM. Anti-HIV-1 and cytotoxicity of a new dimeric thiazepine alkaloid isolated from Ixora undulata Roxb. leaves. Med Chem Res. 2017; 26: 2119–2126. https://doi.org/10.1007/s00044-017-1921-y
  • Chen H, Miao Q, Geng M, Liu J, Hu Y, Tian L, Pan J, Yang Y. Anti-tumor effect of rutin on human neuroblastoma cell lines through inducing G2/M cell cycle arrest and promoting apoptosis. ScientificWorldJournal. 2013; 269165: 1- 8. https://doi.org/10.1155/2013/269165
  • Araújo JR, Gonçalves P, Martel F. Chemopreventive effect of dietary polyphenols in colorectal cancer cell lines. Nutr Res. 2011; 31(2): 77-87. https://doi.org/10.1016/j.nutres.2011.01.006
  • Martínez Conesa C, Vicente Ortega V, Yáñez Gascón MJ, Alcaraz Baños M, Canteras Jordana M, Benavente-García O, Castillo J. Treatment of metastatic melanoma B16F10 by the flavonoids tangeretin, rutin, and diosmin. J Agric Food Chem. 2005; 53(17): 6791-6797. https://doi.org/10.1021/jf058050g
  • Drewa G, Schachtschabel DO, Pałgan K, Grzanka A, Sujkowska R. The influence of rutin on the weight, metastasis, and melanin content of B16 melanotic melanoma in C57BL/6 mice. Neoplasma. 1998; 45(4): 266–271.
  • Cristina Marcarini J, Ferreira Tsuboy MS, Cabral Luiz R, Regina Ribeiro L, Beatriz Hoffmann-Campo C, Ségio Mantovani M. Investigation of cytotoxic, apoptosis-inducing, genotoxic and protective effects of the flavonoid rutin in HTC hepatic cells. Exp Toxicol Pathol. 2011; 63(5): 459-465. https://doi.org/10.1016/j.etp.2010.03.005
  • Hashemzaei M, Delarami Far A, Yari A, Heravi RE, Tabrizian K, Taghdisi SM, Sadegh SE, Tsarouhas K, Kouretas D, Tzanakakis G, Nikitovic D, Anisimov NY, Spandidos DA, Tsatsakis AM, Rezaee R. Anticancer and apoptosis inducing effects of quercetin in vitro and in vivo. Oncol Rep. 2017; 38(2): 819-828. https://doi.org/10.3892/or.2017.5766
  • Salehi B, Machin L, Monzote L, Sharifi-Rad J, Ezzat SM, Salem MA, Merghany RM, El Mahdy NM, Kılıç CS, Sytar O, Sharifi-Rad M, Sharopov F, Martins N, Martorell M, Cho WC. Therapeutic potential of quercetin: New insights and perspectives for human health. ACS Omega. 2020; 5(20): 11849-11872. https://doi.org/10.1021/acsomega.0c01818
  • Venditto VJ, Simanek EE. Cancer therapies utilizing the Camptothecins: a review of the in vivo literature. Mol Pharm. 2010; 7(2): 307-349. https://doi.org/10.1021/mp900243b
  • Wall ME, Wani MC, Cook CE, Palmer KH, McPhail AT, Sim GA. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata. J Am Chem Soc. 1966; 88(16): 3888-3890. https://doi.org/10.1021/ja00968a057
  • Slichenmyer WJ, Von Hoff DD. New natural products in cancer chemotherapy. J Clin Pharmacol. 1990; 30(9): 770- 788. https://doi.org/10.1002/j.1552-4604.1990.tb01873.x
  • Ghoshal DS, Kharat SN, Godbole SA. HPTLC quantification and estimation of rutin and kaempferol using aerial parts of Ixora javanica (Blume) dc. and Ixora barbata Roxb. ex. sm. Res J Pharma Technol. 2022; 15(10): 4533-4541. https://doi.org/10.52711/0974-360X.2022.00761
  • Singh I, Kumaravadivel N, Gnanam R, Vellaikumar S. RP-HPLC analysis for camptothecin content in Nothapodytes nimmoniana, an endangered medicinal plant. J Med Plants Res. 2010; 4(3):255-259.
  • Shamsa F, Monsef H, Ghamooshi R, Verdian-rizi M. Spectrophotometric determination of total alkaloids in some Iranian medicinal plants. Thai J Pharm Sci. 2008; 32(1): 17–20. https://doi.org/10.56808/3027-7922.2196
  • Vijay DT, Rajendra SB. Estimation of Total phenol, tannin, alkaloid and flavonoid in Hibiscus tiliaceus Linn. wood extracts. Research and Reviews: J Pharmacogn Phytochem. 2014; 2 (4): 41-47.
  • Vichai V, Kirtikara K. Sulforhodamine B colorimetric assay for cytotoxicity screening. Nat Protoc. 2006; 1(3): 1112– 1116. https://doi.org/10.1038/nprot.2006.179
  • Caparica R, Júlio A, Araújo MEM, Baby AR, Fonte P, Costa JG, Santos de Almeida T. Anticancer activity of rutin and its combination with ionic liquids on renal cells. Biomolecules. 2020; 10(2): 233. https://doi.org/10.3390/biom10020233
  • Satari A, Ghasemi S, Habtemariam S, Asgharian S, Lorigooini Z. Rutin: A flavonoid as an effective sensitizer for anticancer therapy; insights into multifaceted mechanisms and applicability for combination therapy. Evid Based Complement Alternat Med. 2021; 9913179. https://doi.org/10.1155/2021/9913179
  • Ben Sghaier M, Pagano A, Mousslim M, Ammari Y, Kovacic H, Luis J. Rutin inhibits proliferation, attenuates superoxide production, and decreases adhesion and migration of human cancerous cells. Biomed Pharmacother. 2016; 84: 1972-1978. https://doi.org/10.1016/j.biopha.2016.11.001
  • Vafadar A, Shabaninejad Z, Movahedpour A, Fallahi F, Taghavipour M, Ghasemi Y, Akbari M, Shafiee A, Hajighadimi S, Moradizarmehri S, Razi E, Savardashtaki A, Mirzaei H. Quercetin and cancer: new insights into its therapeutic effects on ovarian cancer cells. Cell Biosci. 2020; 10: 32. https://doi.org/10.1186/s13578-020-00397-0
  • Rauf A, Imran M, Khan IA, Ur-Rehman M, Gilani SA, Mehmood Z, Mubarak MS. Anticancer potential of quercetin: A comprehensive review. Phytother Res. 2018; 32(11): 2109-2130. https://doi.org/10.1002/ptr.6155
  • Imran M, Salehi B, Sharifi-Rad J, Aslam Gondal T, Saeed F, Imran A, Shahbaz M, Tsouh Fokou PV, Umair Arshad M, Khan H, Guerreiro SG, Martins N, Estevinho LM. Kaempferol: A Key Emphasis to Its Anticancer Potential. Molecules. 2019 ;24(12):2277. https://doi.org/10.3390/molecules24122277
  • Amjad E, Sokouti B, Asnaashari S. A systematic review of anti-cancer roles and mechanisms of kaempferol as a natural compound. Cancer Cell Int. 2022; 22(1): 260. https://doi.org/10.1186/s12935-022-02673-0
  • Galatage ST, Trivedi R, Bhagwat DA. Characterization of Camptothecin by analytical methods and determination of anticancer potential against prostate cancer. Futur J Pharm Sci. 2021; 7: 104. https://doi.org/10.1186/s43094-021- 00236-0
  • Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst. 1990; 4; 82(13): 1107-1112. https://doi.org/10.1093/jnci/82.13.1107
  • Kode J, Kovvuri J, Nagaraju B, Jadhav S, Barkume M, Sen S, Kasinathan NK, Chaudhari P, Mohanty BS, Gour J, Sigalapalli DK, Ganesh Kumar C, Pradhan T, Banerjee M, Kamal A. Synthesis, biological evaluation, and molecular docking analysis of phenstatin based indole linked chalcones as anticancer agents and tubulin polymerization inhibitors. Bioorg Chem. 2020; 105: 104447. https://doi.org/10.1016/j.bioorg.2020.104447
  • Kholiya F, Chatterjee S, Bhojani G, Sen S, Barkume M, Kasinathan NK, Kode J, Meena R. Seaweed polysaccharide derived bioaldehyde nanocomposite: Potential application in anticancer therapeutics. Carbohydr Polym. 2020; 240: 116282. https://doi.org/10.1016/j.carbpol.2020.116282

Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach

Year 2025, Volume: 29 Issue: 5, 1823 - 1834, 01.09.2025
https://doi.org/10.12991/jrespharm.1763436

Abstract

Bioactive anticancer compounds like alkaloid camptothecin and flavonoids rutin, quercetin and
kaempferol have been isolated from Ixora coccinea. Being commercially important, research towards finding more plants
with anticancer compounds belonging to genus Ixora is on the forefront. Anti cell proliferative potential of ethanolic
plant part extracts of I. pavetta, I. barbata, I. javanica and I. undulata were studied against three cancer cell lines namely,
Human leukemia cancer cell line K-562, Human breast cancer cell line MDA-MB-231 and Human lung cancer cell line
A-549 using SRB assay. The result of anti-cell proliferative activity is further correlated with the total flavonoid content
of aerial parts and total alkaloid content of underground parts of plants estimated by spectrophotometric assay. The
root extract of I. javanica exhibited the best results with GI50 values of <10 µg/ml against all the three cancer cell lines
studied. Interestingly, the total alkaloid content was also highest in roots of I. javanica possibly pointing some novel
alkaloid to be responsible for its strong anti-cell proliferative activity. Bark extracts of I. javanica, I. pavetta and I. barbata
also exhibited GI50 values of <10 µg/ml specifically against one of the cell lines studied namely - Human leukemia
cancer cell line K-562. All three barks mentioned above also showed higher levels of total alkaloids. This is the first
study reporting the anti-cell proliferative potential of root and bark extracts of I. javanica and I. barbata. These plants
possess in their roots and bark some alkaloids with strong anti-cell proliferative activity which needs further
investigation.

References

  • Baliga MS, Kurian PJ. Ixora coccinea Linn.: Traditional uses, phytochemistry and pharmacology. Chin J Integr Med. 2012; 18(1): 72-79. https://doi.org/10.1007/s11655-011-0881-3
  • Annapurna J, Amarnath PV, Amar Kumar D, Ramakrishna SV, Raghavan KV. Antimicrobial activity of Ixora coccinea leaves. Fitoterapia. 2003; 74(3): 291-293. https://doi.org/10.1016/s0367-326x(03)00037-6
  • Latha PG, Panikkar KR. Cytotoxic and antitumor principles from Ixora coccinea flowers. Cancer Lett. 1998; 130(1-2) :197-202. https://doi.org/10.1016/s0304-3835(98)00140-2
  • Ratnasooriya WD, Deraniyagala SA, Galhena G, Liyanage SS, Bathige SD, Jayakody JR. Anti-inflammatory activity of the aqueous leaf extract of Ixora coccinea. Pharm Biol. 2005;43(2):147-152. https://doi.org/10.1080/13880200590919483
  • Anantharaju PG, Gowda PC, Vimalambike MG, Madhunapantula SV. An overview on the role of dietary phenolics for the treatment of cancers. Nutr J. 2016; 15(1): 99. https://doi.org/10.1186/s12937-016-0217-2
  • Dontha S, Kamurthy H, Manthripragada B. Phytochemical and pharmacological profile of Ixora: A Review. Int J Pharm Sci Res. 2015; 6(2): 567-584. http://doi.org/10.13040/IJPSR.0975-8232.6(2).567-84
  • Lin JP, Yang JS, Lin JJ, Lai KC, Lu HF, Ma CY, Sai-Chuen Wu R, Wu KC, Chueh FS, Gibson Wood W, Chung JG. Rutin inhibits human leukemia tumor growth in a murine xenograft model in vivo. Environ Toxicol. 2012; 27(8): 480– 484. https://doi.org/10.1002/tox.20662
  • Alonso-Castro AJ, Domínguez F, García-Carrancá A. Rutin exerts antitumor effects on nude mice bearing SW480 tumor. Arch Med Res. 2013; 44(5): 346–351. https://doi.org/10.1016/j.arcmed.2013.06.002
  • Yoshida T, Konishi M, Horinaka M, Yasuda T, Goda AE, Taniguchi H, Yano K, Wakada M, Sakai T. Kaempferol sensitizes colon cancer cells to TRAIL-induced apoptosis. Biochem Biophys Res Commun. 2008; 375(1): 129-133. https://doi.org/10.1016/j.bbrc.2008.07.131
  • Davis JM, Murphy EA, Carmichael MD. Effects of the dietary flavonoid quercetin upon performance and health. Curr Sports Med Rep. 2009; 8(4): 206-213. https://doi.org/10.1249/JSR.0b013e3181ae8959
  • Wall ME, Wani MC. Camptothecin and taxol: from discovery to clinic. J Ethnopharmacol. 1996; (1-3): 239-254. https://doi.org/10.1016/0378-8741(95)01367-9
  • Isah T, Umar S. Influencing in vitro clonal propagation of Chonemorpha fragrans (moon) Alston by culture media strength, plant growth regulators, carbon source and photo periodic incubation. J For Res. 2018; 31: 27-43. https://doi.org/10.1007/s11676-018-0794-3
  • Saravanan P, Boopalan E. Occurrence of Camptothecin, an anticancer drug from Ixora coccinea Linn. Int J Appl Biol. 2011; 2(2): 30-34.
  • Kavitha P, Vasantha Kumar T, Rajasekharan PE, Abdul Kareem VK, Rao VK. Camptothecin and 9-methoxy Camptothecin, anti-cancer alkaloids in Nothapodytes nimmoniana from Western Ghats, India. J Med Aromat Plant Sci. 2010; 32(2): 129-132.
  • Ghoshal DS, Kharat SN, Godbole SA. Phytochemical and comparative assessment of bark and root extracts of Ixora barbata Roxb. ex. Sm. and Ixora coccinea L. using high-performance thin layer chromatography assay. Indian J Pharm Sci. 2022; 84(3): 604-616. https://doi.org/10.36468/pharmaceutical-sciences.956
  • Nair SC, Panikkar KR. Antitumor principles from Ixora javanica. Cancer Lett. 1990; 49(2): 121–126. https://doi.org/10.1016/0304-3835(90)90147-p
  • Nair SC, Panikkar B, Akamanchi KG, Panikkar KR. Inhibitory effects of Ixora javanica extract on skin chemical carcinogenesis in mice and its antitumor activity. Cancer Lett. 1991; 60(3): 253–258. https://doi.org/10.1016/0304- 3835(91)90121-w
  • Mohammed M M D, Ibrahim N A, Chen M, Zhai L. Rubiothiazepine a novel unusual cytotoxic alkaloid from Ixora undulata Roxb. leaves. Nat Prod Chem Res. 2014; 2: 128. https://doi.org/10.4172/2329-6836.100012
  • Mohammed MMD, Mohamed KM. Anti-HIV-1 and cytotoxicity of a new dimeric thiazepine alkaloid isolated from Ixora undulata Roxb. leaves. Med Chem Res. 2017; 26: 2119–2126. https://doi.org/10.1007/s00044-017-1921-y
  • Chen H, Miao Q, Geng M, Liu J, Hu Y, Tian L, Pan J, Yang Y. Anti-tumor effect of rutin on human neuroblastoma cell lines through inducing G2/M cell cycle arrest and promoting apoptosis. ScientificWorldJournal. 2013; 269165: 1- 8. https://doi.org/10.1155/2013/269165
  • Araújo JR, Gonçalves P, Martel F. Chemopreventive effect of dietary polyphenols in colorectal cancer cell lines. Nutr Res. 2011; 31(2): 77-87. https://doi.org/10.1016/j.nutres.2011.01.006
  • Martínez Conesa C, Vicente Ortega V, Yáñez Gascón MJ, Alcaraz Baños M, Canteras Jordana M, Benavente-García O, Castillo J. Treatment of metastatic melanoma B16F10 by the flavonoids tangeretin, rutin, and diosmin. J Agric Food Chem. 2005; 53(17): 6791-6797. https://doi.org/10.1021/jf058050g
  • Drewa G, Schachtschabel DO, Pałgan K, Grzanka A, Sujkowska R. The influence of rutin on the weight, metastasis, and melanin content of B16 melanotic melanoma in C57BL/6 mice. Neoplasma. 1998; 45(4): 266–271.
  • Cristina Marcarini J, Ferreira Tsuboy MS, Cabral Luiz R, Regina Ribeiro L, Beatriz Hoffmann-Campo C, Ségio Mantovani M. Investigation of cytotoxic, apoptosis-inducing, genotoxic and protective effects of the flavonoid rutin in HTC hepatic cells. Exp Toxicol Pathol. 2011; 63(5): 459-465. https://doi.org/10.1016/j.etp.2010.03.005
  • Hashemzaei M, Delarami Far A, Yari A, Heravi RE, Tabrizian K, Taghdisi SM, Sadegh SE, Tsarouhas K, Kouretas D, Tzanakakis G, Nikitovic D, Anisimov NY, Spandidos DA, Tsatsakis AM, Rezaee R. Anticancer and apoptosis inducing effects of quercetin in vitro and in vivo. Oncol Rep. 2017; 38(2): 819-828. https://doi.org/10.3892/or.2017.5766
  • Salehi B, Machin L, Monzote L, Sharifi-Rad J, Ezzat SM, Salem MA, Merghany RM, El Mahdy NM, Kılıç CS, Sytar O, Sharifi-Rad M, Sharopov F, Martins N, Martorell M, Cho WC. Therapeutic potential of quercetin: New insights and perspectives for human health. ACS Omega. 2020; 5(20): 11849-11872. https://doi.org/10.1021/acsomega.0c01818
  • Venditto VJ, Simanek EE. Cancer therapies utilizing the Camptothecins: a review of the in vivo literature. Mol Pharm. 2010; 7(2): 307-349. https://doi.org/10.1021/mp900243b
  • Wall ME, Wani MC, Cook CE, Palmer KH, McPhail AT, Sim GA. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata. J Am Chem Soc. 1966; 88(16): 3888-3890. https://doi.org/10.1021/ja00968a057
  • Slichenmyer WJ, Von Hoff DD. New natural products in cancer chemotherapy. J Clin Pharmacol. 1990; 30(9): 770- 788. https://doi.org/10.1002/j.1552-4604.1990.tb01873.x
  • Ghoshal DS, Kharat SN, Godbole SA. HPTLC quantification and estimation of rutin and kaempferol using aerial parts of Ixora javanica (Blume) dc. and Ixora barbata Roxb. ex. sm. Res J Pharma Technol. 2022; 15(10): 4533-4541. https://doi.org/10.52711/0974-360X.2022.00761
  • Singh I, Kumaravadivel N, Gnanam R, Vellaikumar S. RP-HPLC analysis for camptothecin content in Nothapodytes nimmoniana, an endangered medicinal plant. J Med Plants Res. 2010; 4(3):255-259.
  • Shamsa F, Monsef H, Ghamooshi R, Verdian-rizi M. Spectrophotometric determination of total alkaloids in some Iranian medicinal plants. Thai J Pharm Sci. 2008; 32(1): 17–20. https://doi.org/10.56808/3027-7922.2196
  • Vijay DT, Rajendra SB. Estimation of Total phenol, tannin, alkaloid and flavonoid in Hibiscus tiliaceus Linn. wood extracts. Research and Reviews: J Pharmacogn Phytochem. 2014; 2 (4): 41-47.
  • Vichai V, Kirtikara K. Sulforhodamine B colorimetric assay for cytotoxicity screening. Nat Protoc. 2006; 1(3): 1112– 1116. https://doi.org/10.1038/nprot.2006.179
  • Caparica R, Júlio A, Araújo MEM, Baby AR, Fonte P, Costa JG, Santos de Almeida T. Anticancer activity of rutin and its combination with ionic liquids on renal cells. Biomolecules. 2020; 10(2): 233. https://doi.org/10.3390/biom10020233
  • Satari A, Ghasemi S, Habtemariam S, Asgharian S, Lorigooini Z. Rutin: A flavonoid as an effective sensitizer for anticancer therapy; insights into multifaceted mechanisms and applicability for combination therapy. Evid Based Complement Alternat Med. 2021; 9913179. https://doi.org/10.1155/2021/9913179
  • Ben Sghaier M, Pagano A, Mousslim M, Ammari Y, Kovacic H, Luis J. Rutin inhibits proliferation, attenuates superoxide production, and decreases adhesion and migration of human cancerous cells. Biomed Pharmacother. 2016; 84: 1972-1978. https://doi.org/10.1016/j.biopha.2016.11.001
  • Vafadar A, Shabaninejad Z, Movahedpour A, Fallahi F, Taghavipour M, Ghasemi Y, Akbari M, Shafiee A, Hajighadimi S, Moradizarmehri S, Razi E, Savardashtaki A, Mirzaei H. Quercetin and cancer: new insights into its therapeutic effects on ovarian cancer cells. Cell Biosci. 2020; 10: 32. https://doi.org/10.1186/s13578-020-00397-0
  • Rauf A, Imran M, Khan IA, Ur-Rehman M, Gilani SA, Mehmood Z, Mubarak MS. Anticancer potential of quercetin: A comprehensive review. Phytother Res. 2018; 32(11): 2109-2130. https://doi.org/10.1002/ptr.6155
  • Imran M, Salehi B, Sharifi-Rad J, Aslam Gondal T, Saeed F, Imran A, Shahbaz M, Tsouh Fokou PV, Umair Arshad M, Khan H, Guerreiro SG, Martins N, Estevinho LM. Kaempferol: A Key Emphasis to Its Anticancer Potential. Molecules. 2019 ;24(12):2277. https://doi.org/10.3390/molecules24122277
  • Amjad E, Sokouti B, Asnaashari S. A systematic review of anti-cancer roles and mechanisms of kaempferol as a natural compound. Cancer Cell Int. 2022; 22(1): 260. https://doi.org/10.1186/s12935-022-02673-0
  • Galatage ST, Trivedi R, Bhagwat DA. Characterization of Camptothecin by analytical methods and determination of anticancer potential against prostate cancer. Futur J Pharm Sci. 2021; 7: 104. https://doi.org/10.1186/s43094-021- 00236-0
  • Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst. 1990; 4; 82(13): 1107-1112. https://doi.org/10.1093/jnci/82.13.1107
  • Kode J, Kovvuri J, Nagaraju B, Jadhav S, Barkume M, Sen S, Kasinathan NK, Chaudhari P, Mohanty BS, Gour J, Sigalapalli DK, Ganesh Kumar C, Pradhan T, Banerjee M, Kamal A. Synthesis, biological evaluation, and molecular docking analysis of phenstatin based indole linked chalcones as anticancer agents and tubulin polymerization inhibitors. Bioorg Chem. 2020; 105: 104447. https://doi.org/10.1016/j.bioorg.2020.104447
  • Kholiya F, Chatterjee S, Bhojani G, Sen S, Barkume M, Kasinathan NK, Kode J, Meena R. Seaweed polysaccharide derived bioaldehyde nanocomposite: Potential application in anticancer therapeutics. Carbohydr Polym. 2020; 240: 116282. https://doi.org/10.1016/j.carbpol.2020.116282
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Details

Primary Language English
Subjects Pharmaceutical Botany
Journal Section Research Article
Authors

Dipanwita Ghoshal This is me 0009-0008-8883-4486

Sangeeta Godbole This is me 0009-0009-6734-1647

Publication Date September 1, 2025
Submission Date July 16, 2024
Acceptance Date October 29, 2024
Published in Issue Year 2025 Volume: 29 Issue: 5

Cite

APA Ghoshal, D., & Godbole, S. (2025). Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach. Journal of Research in Pharmacy, 29(5), 1823-1834. https://doi.org/10.12991/jrespharm.1763436
AMA Ghoshal D, Godbole S. Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach. J. Res. Pharm. September 2025;29(5):1823-1834. doi:10.12991/jrespharm.1763436
Chicago Ghoshal, Dipanwita, and Sangeeta Godbole. “Exploring the Anti-Cancer Potential of Ixora Extracts: A Multi-Cell Line Approach”. Journal of Research in Pharmacy 29, no. 5 (September 2025): 1823-34. https://doi.org/10.12991/jrespharm.1763436.
EndNote Ghoshal D, Godbole S (September 1, 2025) Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach. Journal of Research in Pharmacy 29 5 1823–1834.
IEEE D. Ghoshal and S. Godbole, “Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach”, J. Res. Pharm., vol. 29, no. 5, pp. 1823–1834, 2025, doi: 10.12991/jrespharm.1763436.
ISNAD Ghoshal, Dipanwita - Godbole, Sangeeta. “Exploring the Anti-Cancer Potential of Ixora Extracts: A Multi-Cell Line Approach”. Journal of Research in Pharmacy 29/5 (September2025), 1823-1834. https://doi.org/10.12991/jrespharm.1763436.
JAMA Ghoshal D, Godbole S. Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach. J. Res. Pharm. 2025;29:1823–1834.
MLA Ghoshal, Dipanwita and Sangeeta Godbole. “Exploring the Anti-Cancer Potential of Ixora Extracts: A Multi-Cell Line Approach”. Journal of Research in Pharmacy, vol. 29, no. 5, 2025, pp. 1823-34, doi:10.12991/jrespharm.1763436.
Vancouver Ghoshal D, Godbole S. Exploring the anti-cancer potential of Ixora extracts: A multi-cell line approach. J. Res. Pharm. 2025;29(5):1823-34.