Metabolomic Approach in Anticancer Biomarker Discovery from Foliose Lichens

Headnote

Keywords:

Lichen, Anticancer, Metabolomics, HeLa, P. caroliniana

Abstract

Purpose: Lichens are well-known as a source of pharmacologically active compounds. This includes anticancer compounds which have biomass constraints including using traditional techniques of lichen bioprospecting. This current study reports the use of cutting-edge metabolomics and a computational approach to discover anticancer biomarkers from Indonesian lichens.

Methods: Seven lichen crude extracts were evaluated against cervical cell lines HeLa using a MTT assay and secondary metabolites were profiled and recorded via a gas chromatography-mass spectrometry (GC-MS) protocol. A multivariate analysis orthogonal partial least-squares-discriminant analysis (OPLS-DA) was employed to determine anticancer biomarker of the lichens. A structure-based computational study against the HeLa cancer cell related protein targets (BCL-2 (4MAN), AKT-1 (4GV1), MCL-1 (5FDO), and BRAF (SVAM)) was used to determine the most potent biomarker.

Results:Jhe MTT assessment indicated the seven lichens possessed strong, medium and weak cytotoxicity. Multivariate analysis showed an OPLS-DA score plot with distinct separation among the strong, medium and weak cytotoxic groups. The biplot OPLS-DA and GC-MS analysis proposed 13 compounds of Parmelia caroliniana and 12 compounds of Physcia cf. millegrana as anticancer biomarker candidates. Docking experiments revealed 6-amino-3,4,7-triphenylpyrido[2',3':4,5]thieno[2,3-c]pyridazine 4 from P. caroliniana to possess the highest binding affinity against BCL-2 (4MAN), AKT-1 (4GV1), MCL-1 (5FDO), and BRAF (5VAM) proteins with affinity energy values of-1 0.0, -11.6, -1 0.4, -12.6, respectively. Conclusion: The study successfully revealed compound 4 as the anticancer biomarker against HeLa cell cancer of P. caroliniana in which can be further explored through in vitro and in vivo studies. Further, the metabolomic protocol established can be adapted as a tool for biomarker discoveries from other medicinal plants.

Introduction

Cervical cancer is a life-threatening disease with a total of 662301 cases resulting in 348874 deaths in 2022.1 Complications and side effects of currently available therapeutic agents demand new strategies for the development of new treatments, including the discovery of new anticancer agents with less side effects and minimal cost.2 Natural products are known as the source for 60% of the currently available anticancer drugs and these include bleomycin sulfate and topotecan hydrochloride, both natural product derivates used in cervical cancer treatment.3 A diversity of organisms have been subjected to anti cervical cancer bioprospecting including the cosmopolitan composite organism, the lichens, which have been used traditionally to treat cancer within numerous cultures around the world.4 Numerous lichen secondary metabolites have been isolated and evaluated for their bioactivities against an array of malignant cell lines.5

However, lichen bioprospecting remains a challenging task due to its limited biomass availability.6 This restraint traditional bioassay guided phytochemical investigation unsuitable. Therefore, a new mean metabolomic approach is necessary as this requires a relatively small amount of sample.7 In this study, a multivariate technique, orthogonal partial least-squares-discriminant analysis (OPLS-DA) was adopted to identify bioactive compounds from selected lichen species which are responsible for their cytotoxicity against HeLa cell line. An in-silico study

was performed to confirm the anticancer biomarkers.

Material and Method

Lichen collection and extraction

Seven foliose lichen samples were collected from East Java, Indonesia including Parmelia aurulenta Tuck, from Jember district, Parmelia caroliniana Nyl. from Pasuruan district, Parmelia cetrata Ach., Parmelia dilatata Vain., Cladonia scabriuscula (Duby) Leight, Candelaria fibrosa (Fr.) Mull. Arg., and Physcia cf. millegrana Degel. from Bondowoso district. Samples were stored and labelled at the Drug Utilisation and Discovery Research Group (DUDRG), Faculty of Pharmacy, University of Jember, Indonesia. Dried lichen samples were ground in the presence of liquid nitrogen and were then extracted with methanol followed by vacuum drying to produce crude methanol extracts.

Anticancer bioassay

Cytotoxicity was measured using a standard MTT assay8 HeLa (ATCC CRM-CCL-2) cells were treated with serial concentrations of lichen extracts (1024, 512, 256, 128, 64, 32 ug/mL).

Metabolomics experiment

Metabolomic profiles were generated based on a standard gas chromatography-mass spectrometry (GC-MS) protocol developed by Lisec at al.9 Compound annotation was generated from spectral data comparison against the mass spectra library, NIST version 2.2. Metabolomicstu dies were conducted usingthe multivariate analysis software SIMCA by MKS UMETRICS. The data used comprised of the x-axis representing the area at a specific retention time with the y-axis defining the lichen species. Chromatograms were pre-processed to produce 58 binned data and the lichens were classified into 3 groups based on cytotoxicity (IC values). Multivariate analysis was performed using the OPLS-DA method.

Computational study

Biomarker candidates were investigated using AutoDock Vina vl.2.3 on the HeLa related protein targets BCL-2 (PDBID:4MAN),MCL-1 (PDBID: 5FDO),AKT-l (PDB ID: 4GV1) and BRAF (PDB ID: 5VAM) with respective positive controls, 1Y1, 5X2, OXZ and 92J. Molecular energy minimisation and format conversion into pdbqt were performed using ChemBio and MGLTools software 1.5.7., respectively. The best docking conformations were imported and their interactions were evaluated using BIO VIA Discovery Visualizer v21.1.0.20298.

Results and Discussion

Lichen secondary metabolites were extracted from seven foliose lichen species using methanol with molecule derivatisation conducted using N-methyl trifluoroacetamide (MSTFA) to enable robust molecular detection in the GC-MS. The cytotoxicity bioassay indicated HeLa cell lines to possess various sensitivities against the seven-lichens with P. millegrana showing the highest activity (Table 1).

A multivariate analysis using OPLS-DA produced good separation between the classified groups as depicted in both 2D score plots (Figure 1). The least active groups (red) including C. fibrosa, P. cetrata and P. dilatata were all gathered in the left quadrant with the medium (blue dots) and active groups (green dots) in the right quadrant (Figure 2, top). Further analysis based on a biplot diagram, an overlayed score and loading plot, displayed a distinct distribution of loading plot (yellow dots, represents the retention time generated from GC-MS chromatogram) around P. caroliniana and P. millegrana plots (Figure 2, bottom). This biplot analysis facilitated in determining important variables (retention time) which contribute to the anticancer activity of P. caroliniana (13.5-13.99; 20.5-20,99; 30-30.49 min) and P. millegrana (7.5-7.99; 8.5-8.99; 11.5-11.99; 13.5-13.99; 16-16.49; 18-18.49; 19.5 min). GC-MS compound annotation led to molecular identification of 13 secondary metabolites of P. caroliniana and 12 secondary metabolites of P. millegrana which correlated to cytotoxicity.

The in-silico investigation on 25 compounds of P millegrana and P caroliniana generated from OPLSDA multivariate analysis was performed using a docking approach with proteins related to cervical cancer, B-cell lymphoma-2 protein (BCL-2, PDB ID: 4MAN), alpha kinase threonin-1 protein (AKT-1, PDB ID: 4GV1), myeloid cell leukemia-1 protein (MCL-1, PDB ID: 5FDO), and V-raf murine sarcoma viral oncogene homolog Bl protein (BRAF, PDB ID: 5VAM) (Table 2). The docking experiment revealed 12 metabolites of P. millegrana to possess insignificant binding energy towards all four proteins compared to the binding affinity of corresponding endogenous ligands. In contrast, compounds 1-7 of P caroliniana showed binding affinities comparative to the endogenous ligands that bind 4GV1, 5FDO and 5VAM proteins. None of the secondary metabolites produced significant interactions against the BCL-2 (4MAN) protein.

The high binding affinity of compound 4 against

AKT-1 (4GV1) resulted from n and conventional hydrogen bond interactions with amino acid residues (Figure 3A). Compound 4 also showed n, van der Waals and conventional hydrogen bonds against MCL-1 protein (5FDO) (Figure 3B). In addition, n binding was responsible for the interaction between compound 4 and BRAF protein (5VAM) (Figure 3C). Overall these interactions and the molecular size of compound 4 followed Lipinskis rule, thus providing reasonable values for pharmacokinetic parameters in drug development.10

Conclusion

The study successfully determined secondary metabolites of P. caroliniana and P. millegrana to have significant cytotoxicity contributions based on OPLS-DA analysis. Computational approaches suggested compound 4 of P. caroliniana as a biomarker compound responsible for the cytotoxicity against HeLa-cell protein marker. This straightforward protocol can be applied in biomarker discovery in other medicinal plants without excessive phytochemical experiments.

Acknowledgments

The authors acknowledge the support of University of Jember through internal research grant.

Authors' Contribution

Conceptualization: Ari Satia Nugraha.

Methodology: Ari Satia Nugraha.

Data curation: Chintya Permata Zahky Sukrisno Putri, Dinar Mutia

Rani, Banun Kusumawardani.

Formal analysis: Chintya Permata Zahky Sukrisno Putri, Dinar

Mutia Rani, Anang Kurnia, Ari Satia Nugraha.

Investigation: Chintya Permata Zahky Sukrisno Putri, Dinar Mutia

Rani, Banun Kusumawardani, Ludmilla Fitri Untari, Anang Kurnia,

Ari Satia Nugraha.

Software: Ari Satia Nugraha, Anang Kurnia.

Supervision: Paul A. Keller, Ari Satia Nugraha.

Validation: Anang Kurnia, Paul A. Keller, Ari Satia Nugraha.

Visualization: Chintya Permata Zahky Sukrisno Putri, Dinar Mutia

Rani, Ari Satia Nugraha.

Funding acquisition: Ari Satia Nugraha.

Writing-original draft: Chintya Permata Zahky Sukrisno Putri,

Dinar Mutia Rani, Ari Satia Nugraha.

Writing-review & editing: Paul A. Keller, Ari Satia Nugraha.

Competing Interests

None.

Ethical Approval

Not applicable.

Funding

The research is funded by University Jember through international cooperation research grant with contract no. 3148/UN25.3.1/ LT/2024.

References

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