Skip to content
2000
image of Anticancer Potential of Eudesmanolides Derived from Sphagneticola trilobata against Colorectal Cancer, by Targeting β-catenin Signalling

Abstract

Introduction

The role of β-catenin signalling in the pathogenesis of Colorectal Cancer (CRC) is indisputable. In this study, we report the identification of a cytotoxic fraction that targets the β-catenin signalling axis in colorectal cancer cells.

Methods

Chromatographic and spectrometric techniques were used for the isolation and phytochemical characterization of Eudesmanolides (EDS). Cell-viability assays, flow cytometry, fluorescent microscopy, immunoblot analysis, qRT-PCR, and molecular docking studies were used to analyse the antitumor potential of EDS against CRC cells. Toxicological evaluation of EDS was conducted in Swiss albino mice.

Results

We have isolated and characterized the bioactive fraction designated EDS, consisting of the eudesmanolides, namely wedelolide D and prostrolide A, from the Ethyl Acetate (EA) leaf extract of the plant (). EDS was found to be highly efficacious against CRC cells and induced an apoptotic mode of cell death in different CRC cell lines. Delineation of the apoptotic pathway induced by EDS revealed extrinsic pathway activation and amplification of the apoptotic signals the intrinsic pathway through truncated-BID. Molecular investigations revealed EDS-mediated inhibition of β-catenin signalling and PPAR-γ (peroxisome proliferator-activated receptor gamma) activation in HCT116 CRC cells.

Discussion

Our study revealed that EDS induced strong apoptotic signals in CRC cells, initiated at the cell surface, resulting in apoptosis involving extrinsic and intrinsic mechanisms irrespective of the p53 status or molecular phenotype of CRC cells. In addition, PPAR-γ activation by EDS resulted in the suppression of β-catenin nuclear accumulation and the subsequent inhibition of proliferative and survival signalling. Moreover, EDS was found to be pharmacologically safe.

Conclusion

To summarize, we demonstrate, with mechanism-based evidence, the chemotherapeutic efficacy of EDS, comprising the eudesmanolides, wedelolide D, and prostrolide A, derived from , against CRC. The potential of these lead-structures are worth exploring for their beneficial effects in combination with other therapeutic interventions.

Loading

Article metrics loading...

/content/journals/acamc/10.2174/0118715206431960260123110937
2026-04-29
2026-05-19
Loading full text...

Full text loading...

References

  1. Sathishkumar K. Chaturvedi M. Das P. Stephen S. Mathur P. Cancer incidence estimates for 2022 & projection for 2025. Indian J. Med. Res. 2022 156 45 598 607 10.4103/ijmr.ijmr_1821_22 36510887
    [Google Scholar]
  2. Murphy N. Moreno V. Hughes D.J. Vodicka L. Vodicka P. Aglago E.K. Gunter M.J. Jenab M. Lifestyle and dietary environmental factors in colorectal cancer susceptibility. Mol. Aspects Med. 2019 69 2 9 10.1016/j.mam.2019.06.005 31233770
    [Google Scholar]
  3. Ahmed D. Eide P.W. Eilertsen I.A. Danielsen S.A. Eknæs M. Hektoen M. Lind G.E. Lothe R.A. Epigenetic and genetic features of 24 colon cancer cell lines. Oncogenesis 2013 2 9 e71 e71 10.1038/oncsis.2013.35 24042735
    [Google Scholar]
  4. Ahmad R. Singh J. Wunnava A. Al-Obeed O. Abdulla M. Srivastava S. Emerging trends in colorectal cancer: Dysregulated signaling pathways (Review). Int. J. Mol. Med. 2021 47 3 14 10.3892/ijmm.2021.4847 33655327
    [Google Scholar]
  5. Mortezaee K. WNT/β-catenin regulatory roles on PD-(L)1 and immunotherapy responses. Clin. Exp. Med. 2024 24 1 15 10.1007/s10238‑023‑01274‑z 38280119
    [Google Scholar]
  6. Song P. Gao Z. Bao Y. Chen L. Huang Y. Liu Y. Dong Q. Wei X. Wnt/β-catenin signaling pathway in carcinogenesis and cancer therapy. J. Hematol. Oncol. 2024 17 1 46 10.1186/s13045‑024‑01563‑4 38886806
    [Google Scholar]
  7. Vallée A. Lecarpentier Y. Crosstalk between peroxisome proliferator-activated receptor gamma and the canonical WNT/β-catenin pathway in chronic inflammation and oxidative stress during carcinogenesis. Front. Immunol. 2018 9 745 10.3389/fimmu.2018.00745 29706964
    [Google Scholar]
  8. Liu J. Wang H. Zuo Y. Farmer S.R. Functional interaction between peroxisome proliferator-activated receptor γ and β-catenin. Mol. Cell. Biol. 2006 26 15 5827 5837 10.1128/MCB.00441‑06 16847334
    [Google Scholar]
  9. Chinetti G. Fruchart J.C. Staels B. Peroxisome proliferator-activated receptors (PPARs): Nuclear receptors at the crossroads between lipid metabolism and inflammation. Inflamm. Res. 2000 49 10 497 505 10.1007/s000110050622 11089900
    [Google Scholar]
  10. Aboonabi A. Aboonabi A. Anthocyanins reduce inflammation and improve glucose and lipid metabolism associated with inhibiting nuclear factor-kappaB activation and increasing PPAR-γ gene expression in metabolic syndrome subjects. Free Radic. Biol. Med. 2020 150 30 39 10.1016/j.freeradbiomed.2020.02.004 32061902
    [Google Scholar]
  11. Dubuquoy L. Rousseaux C. Thuru X. Peyrin-Biroulet L. Romano O. Chavatte P. Chamaillard M. Desreumaux P. PPAR as a new therapeutic target in inflammatory bowel diseases. Gut 2006 55 9 1341 1349 10.1136/gut.2006.093484 16905700
    [Google Scholar]
  12. Sarraf P. Mueller E. Smith W.M. Wright H.M. Kum J.B. Aaltonen L.A. de la Chapelle A. Spiegelman B.M. Eng C. Loss-of-function mutations in PPAR γ associated with human colon cancer. Mol. Cell 1999 3 6 799 804 10.1016/S1097‑2765(01)80012‑5 10394368
    [Google Scholar]
  13. Bandera Merchan B. Tinahones F.J. Macías-González M. Commonalities in the association between PPARG and vitamin D related with obesity and carcinogenesis. PPAR Res. 2016 2016 1 1 15 10.1155/2016/2308249 27579030
    [Google Scholar]
  14. Chen Y. Chen M. Deng K. Blocking the Wnt/β catenin signaling pathway to treat colorectal cancer: Strategies to improve current therapies (Review). Int. J. Oncol. 2022 62 2 24 10.3892/ijo.2022.5472 36579676
    [Google Scholar]
  15. McQuade R.M. Stojanovska V. Bornstein J.C. Nurgali K. Colorectal cancer chemotherapy: the evolution of treatment and new approaches. Curr. Med. Chem. 2017 24 15 1537 1557 [PMID: 28079003
    [Google Scholar]
  16. Hossain M.S. Karuniawati H. Jairoun A.A. Urbi Z. Ooi D.J. John A. Lim Y.C. Kibria K.M.K. Mohiuddin A.K.M. Ming L.C. Goh K.W. Hadi M.A. Colorectal cancer: a review of carcinogenesis, global epidemiology, current challenges, risk factors, preventive and treatment strategies. Cancers 2022 14 7 1732 10.3390/cancers14071732 35406504
    [Google Scholar]
  17. Newman D.J. Cragg G.M. Natural products as sources of new drugs over the nearly four decades from 01/1981 to 09/2019. J. Nat. Prod. 2020 83 3 770 803 10.1021/acs.jnatprod.9b01285 32162523
    [Google Scholar]
  18. Ali M.T. Al-Mahdy D.A. Fishawy A.M.E. Otify A.M. Sphagneticola trilobata (L.) Pruski: An updated exploration of its traditional applications, taxonomy, phytochemical profile and pharmacological properties. S. Afr. J. Bot. 2024 174 183 207 10.1016/j.sajb.2024.08.060
    [Google Scholar]
  19. Aiswarya S.U.D. Vikas G. Haritha N.H. Liju V.B. Shabna A. Swetha M. Rayginia T.P. Keerthana C.K. Nath L.R. Reshma M.V. Sundaram S. Anto N.P. Lankalapalli R.S. Anto R.J. Bava S.V. Corrigendum: Cucurbitacin B, purified and characterized from the rhizome of Corallocarpus epigaeus exhibits anti-melanoma potential. Front. Oncol. 2022 12 989283 10.3389/fonc.2022.989283 36033534
    [Google Scholar]
  20. Athikkavil F.M. Aiswarya S.U. Johny R. Sudhesh M. Nisthul A.A. Lankalapalli R.S. Anto R.J. Bava S.V. A potent bioactive fraction against colon cancer from Plectranthus vettiveroides. Explor. Target. Antitumor Ther. 2023 4 2 227 239 10.37349/etat.2023.00131 37205312
    [Google Scholar]
  21. Glide 2018 Available from: https://www.schrodinger.com/platform/products/glide/
  22. Prime 2018 Available from: https://www.schrodinger.com/platform/products/prime/
  23. Induced Fit Docking protocol. New York, NY Glide, Schrödinger, LLC 2018
    [Google Scholar]
  24. Li Y. Hao X. Li S. He H. Yan X. Chen Y. Dong J. Zhang Z. Li S. Eudesmanolides from Wedelia trilobata (L.) Hitchc. as potential inducers of plant systemic acquired resistance. J. Agric. Food Chem. 2013 61 16 3884 3890 10.1021/jf400390e 23537063
    [Google Scholar]
  25. Abdjul D.B. Yamazaki H. Maarisit W. Losung F. Rotinsulu H. Wewengkang D.S. Sumilat D.A. Namikoshi M. Eudesmanolide sesquiterpenes and protein tyrosine phosphatase 1B inhibitory ent -kaurene diterpenes from aerial parts of Indonesian Wedelia prostata. Phytochem. Lett. 2017 20 191 195 10.1016/j.phytol.2017.04.018
    [Google Scholar]
  26. Sato H. Ishihara S. Kawashima K. Moriyama N. Suetsugu H. Kazumori H. Okuyama T. Rumi M A K. Fukuda R. Nagasue N. Kinoshita Y. Expression of peroxisome proliferator-activated receptor (PPAR)γ in gastric cancer and inhibitory effects of PPARγ agonists. Br. J. Cancer 2000 83 10 1394 1400 10.1054/bjoc.2000.1457 11044367
    [Google Scholar]
  27. Miyamae Y. Insights into dynamic mechanism of ligand binding to peroxisome proliferator-activated receptor γ toward potential pharmacological applications. Biol. Pharm. Bull. 2021 44 9 1185 1195 10.1248/bpb.b21‑00263 34471046
    [Google Scholar]
  28. Garcia-Vallvé S. Guasch L. Tomas-Hernández S. del Bas J.M. Ollendorff V. Arola L. Pujadas G. Mulero M. Peroxisome proliferator-activated receptor γ (PPARγ) and ligand choreography: Newcomers take the stage. J. Med. Chem. 2015 58 14 5381 5394 10.1021/jm501155f 25734377
    [Google Scholar]
  29. de Groot J.C. Weidner C. Krausze J. Kawamoto K. Schroeder F.C. Sauer S. Büssow K. Structural characterization of amorfrutins bound to the peroxisome proliferator-activated receptor γ. J. Med. Chem. 2013 56 4 1535 1543 10.1021/jm3013272 23286787
    [Google Scholar]
  30. Bruning J.B. Chalmers M.J. Prasad S. Busby S.A. Kamenecka T.M. He Y. Nettles K.W. Griffin P.R. Partial agonists activate PPARgamma using a helix 12 independent mechanism. Structure 2007 15 10 1258 1271 10.1016/j.str.2007.07.014 17937915
    [Google Scholar]
  31. Montanari R. Capelli D. Tava A. Galli A. Laghezza A. Tortorella P. Loiodice F. Pochetti G. Screening of saponins and sapogenins from Medicago species as potential PPARγ agonists and X-ray structure of the complex PPARγ/caulophyllogenin. Sci. Rep. 2016 6 1 27658 10.1038/srep27658 27283034
    [Google Scholar]
  32. Wang L. Waltenberger B. Pferschy-Wenzig E.M. Blunder M. Liu X. Malainer C. Blazevic T. Schwaiger S. Rollinger J.M. Heiss E.H. Schuster D. Kopp B. Bauer R. Stuppner H. Dirsch V.M. Atanasov A.G. Natural product agonists of peroxisome proliferator-activated receptor gamma (PPARγ): a review. Biochem. Pharmacol. 2014 92 1 73 89 10.1016/j.bcp.2014.07.018 25083916
    [Google Scholar]
  33. Zhou X.Q. Mao X.M. Fan R. Li S.Y. Shang J. Zhang T. Li R.H. Li H.Q. Hui Y. Chen W.H. Wang Z.X. Shen D.Y. Trilobolide‐6‐O ‐isobutyrate suppresses hepatocellular carcinoma tumorigenesis through inhibition of IL ‐6/ STAT3 signaling pathway. Phytother. Res. 2021 35 10 5741 5753 10.1002/ptr.7233 34355433
    [Google Scholar]
  34. Sun L. Wang Z. Wang Y. Xu J. He X. Anti-proliferative and anti-neuroinflammatory eudesmanolides from Wedelia (Sphagneticola trilobata (L.) Pruski). Fitoterapia 2020 142 104452 10.1016/j.fitote.2019.104452 31857180
    [Google Scholar]
  35. Zhang B. Wang L. Wang L. Wang Y. Xu J. He X. Anti-proliferative and anti-inflammatory eudesmanolides from the flowers of Sphagneticola trilobata (L.) Pruski. Phytochemistry 2023 210 113666 10.1016/j.phytochem.2023.113666 37003362
    [Google Scholar]
  36. Wu G.X. Zhao H.Y. Peng C. Liu F. Xiong L. Eudesmane-type sesquiterpenoids: Structural diversity and biological activity. Heliyon 2024 10 15 e35270 10.1016/j.heliyon.2024.e35270 39170406
    [Google Scholar]
  37. Jeught K.V. Xu H.C. Li Y.J. Lu X.B. Ji G. Drug resistance and new therapies in colorectal cancer. World J. Gastroenterol. 2018 24 34 3834 3848 10.3748/wjg.v24.i34.3834 30228778
    [Google Scholar]
  38. Hashem S. Ali T.A. Akhtar S. Nisar S. Sageena G. Ali S. Al-Mannai S. Therachiyil L. Mir R. Elfaki I. Mir M.M. Jamal F. Masoodi T. Uddin S. Singh M. Haris M. Macha M. Bhat A.A. Targeting cancer signaling pathways by natural products: Exploring promising anti-cancer agents. Biomed. Pharmacother. 2022 150 113054 10.1016/j.biopha.2022.113054 35658225
    [Google Scholar]
  39. Perillo B. Di Donato M. Pezone A. Di Zazzo E. Giovannelli P. Galasso G. Castoria G. Migliaccio A. ROS in cancer therapy: the bright side of the moon. Exp. Mol. Med. 2020 52 2 192 203 10.1038/s12276‑020‑0384‑2 32060354
    [Google Scholar]
  40. Network C.G.A. Comprehensive molecular characterization of human colon and rectal cancer. Nature 2012 487 7407 330 337 10.1038/nature11252 22810696
    [Google Scholar]
  41. Hon K.W. Zainal Abidin S.A. Othman I. Naidu R. The crosstalk between signaling pathways and cancer metabolism in colorectal cancer. Front. Pharmacol. 2021 12 768861 10.3389/fphar.2021.768861 34887764
    [Google Scholar]
  42. Cheng I. Caberto C.P. Lum-Jones A. Seifried A. Wilkens L.R. Schumacher F.R. Monroe K.R. Lim U. Tiirikainen M. Kolonel L.N. Henderson B.E. Stram D.O. Haiman C.A. Le Marchand L. Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies. Gut 2011 60 12 1703 1711 10.1136/gut.2011.237727 21602532
    [Google Scholar]
  43. Sabatino L. Pancione M. Votino C. Colangelo T. Lupo A. Novellino E. Lavecchia A. Colantuoni V. Emerging role of the β-catenin-PPARγ axis in the pathogenesis of colorectal cancer. World J. Gastroenterol. 2014 20 23 7137 7151 10.3748/wjg.v20.i23.7137 24966585
    [Google Scholar]
  44. Lu D. Carson D.A. Repression of β-catenin signaling by PPARγ ligands. Eur. J. Pharmacol. 2010 636 1-3 198 202 10.1016/j.ejphar.2010.03.010 20303941
    [Google Scholar]
  45. Sharma C. Pradeep A. Wong L. Rana A. Rana B. Peroxisome proliferator-activated receptor γ activation can regulate β-catenin levels via a proteasome-mediated and adenomatous polyposis coli-independent pathway. J. Biol. Chem. 2004 279 34 35583 35594 10.1074/jbc.M403143200 15190077
    [Google Scholar]
  46. Girnun G.D. Smith W.M. Drori S. Sarraf P. Mueller E. Eng C. Nambiar P. Rosenberg D.W. Bronson R.T. Edelmann W. Kucherlapati R. Gonzalez F.J. Spiegelman B.M. APC-dependent suppression of colon carcinogenesis by PPARγ. Proc. Natl. Acad. Sci. 2002 99 21 13771 13776 10.1073/pnas.162480299 12370429
    [Google Scholar]
  47. Vallée A. Lecarpentier Y. Guillevin R. Vallée J.N. Opposite interplay between the canonical WNT/β-catenin pathway and PPAR gamma: a potential therapeutic target in gliomas. Neurosci. Bull. 2018 34 3 573 588 10.1007/s12264‑018‑0219‑5 29582250
    [Google Scholar]
  48. Vasconcelos-dos-Santos A. Loponte H F B.R. Mantuano N.R. Oliveira I.A. de Paula I.F. Teixeira L.K. de-Freitas-Junior J.C.M. Gondim K.C. Heise N. Mohana-Borges R. Morgado-Díaz J.A. Dias W.B. Todeschini A.R. Hyperglycemia exacerbates colon cancer malignancy through hexosamine biosynthetic pathway. Oncogenesis 2017 6 3 e306 e306 10.1038/oncsis.2017.2 28319096
    [Google Scholar]
  49. Wu Z.N. Zhang Y.B. Chen N.H. Yang L. Jiang L. Jiang S.Q. Li G.Q. Li Y.L. Wang G.C. Three new eudesmanolides from the herbs of Wedelia prostrata. Chem. Lett. 2016 45 10 1150 1152 10.1246/cl.160546
    [Google Scholar]
  50. Batlle E. Henderson J.T. Beghtel H. van den Born M.M.W. Sancho E. Huls G. Meeldijk J. Robertson J. van de Wetering M. Pawson T. Clevers H. β-catenin and TCF mediate cell positioning in the intestinal epithelium by controlling the expression of EphB/ephrinB. Cell 2002 111 2 251 263 10.1016/S0092‑8674(02)01015‑2 12408869
    [Google Scholar]
  51. Chen S. Guttridge D.C. You Z. Zhang Z. Fribley A. Mayo M.W. Kitajewski J. Wang C.Y. Wnt-1 signaling inhibits apoptosis by activating β-catenin/T cell factor-mediated transcription. J. Cell Biol. 2001 152 1 87 96 10.1083/jcb.152.1.87 11149923
    [Google Scholar]
/content/journals/acamc/10.2174/0118715206431960260123110937
Loading
/content/journals/acamc/10.2174/0118715206431960260123110937
Loading

Data & Media loading...


  • Article Type:
    Research Article
Keywords: asteraceae ; PPAR-γ ; Sphagneticola trilobata ; colorectal cancer ; apoptosis ; eudesmanolides ; β-catenin
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test