Aquilaria crassna leaf extract selectively upregulated calreticulin surface expression, a pro-phagocytotic signal, in triple-negative breast cancer cells
DOI:
https://doi.org/10.14456/nujst.2023.14Keywords:
A. crassna leaf extract, immunogenic modulation, sublethal dose, ectoCRT, triple-negative breast cancerAbstract
During the last decade, studies of anti-cancer properties of extracts from several parts of Aquilaria species including Aquilaria crassna (A. crassna) Pierre ex Lecomte have been more attractive. Leaf extract of A. crassna Pierre ex Lecomte (AE) has been reported for medicinal activities except for anti-cancer activity in particular the enhancement of cancer-immune responses. Strategies that alter cancer phenotypes to be more sensitive to immune cell killing and/or to activate immune responses have become promising approaches for cancer therapy. We are interested in a strategy that sensitizes surviving cancer cells to express surface molecules for the enhancement of cancer cell killing by immune cells called immunogenic modulation. Thereby, this study aims to investigate the induction effect of AE on the expression of molecules reported for immunogenic modulation which are the surface expressions of calreticulin (ectoCRT), a major histocompatibility complex class I (MHC class I), and CD95/Fas death receptor. M.D. Anderson-Metastatic Breast 231 (MDA-MB 231) cell line, a triple-negative breast cancer; TNBC, was treated with various concentrations (0- 640 µg/ml) of AE for 6 hr and 12 hr and examined for the cytotoxic effect by MTT assay. The results showed that concentrations of 20-640 µg/ml of AE treatment significantly decreased the percentages of cell viability at both time points. Sublethal doses (20-320 µg/ml) caused the cell viability > 70% were further examined for the surface expressions of ectoCRT, MHC class I, and CD95 using surface immunostaining and analyzed by flow cytometer. At 12 hr after treatment, AE selectively induced ectoCRT expression but did not show any effect on MHC class I and CD95 expressions in all AE-treated populations. To further clarify the involvement of AE-induced ectoCRT in an immunogenic modulation, AE-treated living cells were chosen to investigate the expression of ectoCRT. Our results found that AE-treated living cells showed a significant increase in the relative mean fluorescence intensity (relative MFI) of ectoCRT expression and a trend to increase in ectoCRT-positive cells compared to the untreated group (0 µg/ml). Together, this is the preliminary result reporting the upregulation of ectoCRT expression by AE. In addition, AE-induced ectoCRT has been mainly found in surviving/living cells which is accorded to the criteria of immunogenic modulation. However, the role of AE-induced ectoCRT in the enhancement of cancer cell killing especially in immune cell phagocytosis needs to be further investigated.
References
Abbas, P., Hashim, Y., & Salleh, H. M. (2019). Uninfected agarwood branch extract possess cytotoxic and inhibitory effects on MCF-7 breast cancer cells. Journal of Research in Pharmacy, 23(1), 120-129. https://doi.org/10.12991/jrp.2018.116
Adam, A. Z., Lee, S. Y., & Mohamed, R. (2017). Pharmacological properties of agarwood tea derived from Aquilaria (Thymelaeaceae) leaves: An emerging contemporary herbal drink. Journal of Herbal Medicine, 10, 37-44. https://doi.org/10.1016/j.hermed.2017.06.002
Agrawal, S., & Kishore, M. C. (2000). MHC class I gene expression and regulation. Journal of Hematotherapy & Stem Cell Research, 9(6), 795-812. https://doi.org/10.1089/152581600750062237
Bauer, K. R., Brown, M., Cress, R. D., Parise, C. A., & Caggiano, V. (2007). Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from the California cancer Registry. Cancer, 109(9), 1721-1728. https://doi.org/10.1002/cncr.22618
Campoli, M., & Ferrone, S. (2008). HLA antigen changes in malignant cells: epigenetic mechanisms and biologic significance. Oncogene, 27(45), 5869-5885. https://doi.org/10.1038/onc.2008.273
Deng, L. J., Qi, M., Li, N., Lei, Y. H., Zhang, D. M., & Chen, J. X. (2020). Natural products and their derivatives: Promising modulators of tumor immunotherapy. Journal of Leukocyte Biology, 108(2), 493-508. https://doi.org/10.1002/JLB.3MR0320-444R
Fabian, K. P., Wolfson, B., & Hodge, J. W. (2021). From Immunogenic Cell Death to Immunogenic Modulation: Select Chemotherapy Regimens Induce a Spectrum of Immune-Enhancing Activities in the Tumor Microenvironment. Frontiers in Oncology, 11, 728018. https://doi.org/10.3389/fonc.2021.728018
Feng, J., Yang, X. W., & Wang, R. F. (2011). Bio-assay guided isolation and identification of alpha-glucosidase inhibitors from the leaves of Aquilaria sinensis. Phytochemistry, 72(2-3), 242-247. https://doi.org/10.1016/j.phytochem.2010.11.025
Fucikova, J., Spisek, R., Kroemer, G., & Galluzzi, L. (2021). Calreticulin and cancer. Cell Research, 31(1), 5-16. https://doi.org/10.1038/s41422-020-0383-9
Galluzzi, L., Vitale, I., Warren, S., Adjemian, S., Agostinis, P., Martinez, A. B., . . . Marincola, F. M. (2020). Consensus guidelines for the definition, detection and interpretation of immunogenic cell death. The Journal for ImmunoTherapy of Cancer, 8(1), e000337. https://doi.org/10.1136/jitc-2019-000337
Ghan, S. Y., Chin, J. H., Thoo, Y. Y., Yim, H. S., & Ho, C. W. (2016). Acute oral toxicity study of Aquilaria Acrassna and α-TOCOPHEROL in mice. International Journal of Pharmaceutical Sciences and Research, 4, 1456-1461. https://doi.org/10.13040/IJPSR.0975-8232.7(4).1456-61
Ghoncheh, M., Pournamdar, Z., & Salehiniya, H. (2016). Incidence and Mortality and Epidemiology of Breast Cancer in the World. Asian Pacific Journal of Cancer Prevention, 17(S3), 43-46. https://doi.org/10.7314/apjcp.2016.17.s3.43
Hashim, Y. Z., Kerr, P. G., Abbas, P., & Mohd Salleh, H. (2016). Aquilaria spp. (agarwood) as source of health beneficial compounds: A review of traditional use, phytochemistry and pharmacology. Journal of Ethnopharmacology, 189, 331-360. https://doi.org/10.1016/j.jep.2016.06.055
Hodge, J. W., Garnett, C. T., Farsaci, B., Palena, C., Tsang, K. Y., Ferrone, S., & Gameiro, S. R. (2013a). Chemotherapy-induced immunogenic modulation of tumor cells enhances killing by cytotoxic T lymphocytes and is distinct from immunogenic cell death. International Journal of Cancer, 133(3), 624-636. https://doi.org/10.1002/ijc.28070
Hodge, J. W., Garnett, C. T., Farsaci, B., Palena, C., Tsang, K. Y., Ferrone, S., & Gameiro, S. R. (2013b). Chemotherapy-induced immunogenic modulation of tumor cells enhances killing by cytotoxic T lymphocytes and is distinct from immunogenic cell death. International Journal of Cancer, 133(3), 624-636. https://doi.org/10.1002/ijc.28070
Jang, H. M., Lee, J. H., Kim, J. H., Park, G., & Jeon, J. H. (2020). In vitro anticancer effect of Aquilaria crassna extract on human mammary gland cancer cells. International journal of Biosciences, 16(4), 187-192. https://doi.org/10.12692/ijb/16.4.187-192
Kakino, M., Tazawa, S., Maruyama, H., Tsuruma, K., Araki, Y., Shimazawa, M., & Hara, H. (2010). Laxative effects of agarwood on low-fiber diet-induced constipation in rats. BMC Complementary and Alternative Medicine, 10, 68. https://doi.org/10.1186/1472-6882-10-68
Kamonwannasit, S., Nantapong, N., Kumkrai, P., Luecha, P., Kupittayanant, S., & Chudapongse, N. (2013). Antibacterial activity of Aquilaria crassna leaf extract against Staphylococcus epidermidis by disruption of cell wall. Annals of Clinical Microbiology and Antimicrobials, 12, 20. https://doi.org/10.1186/1476-0711-12-20
Li, S., Jin, S., Chen, W., Yu, J., Fang, P., Zhou, G., . . . Pan, C. (2020). Mangiferin alleviates endoplasmic reticulum stress in acute liver injury by regulating the miR-20a/miR-101a-Nrf2 axis. Journal of Biochemistry, 168(4), 365-374. https://doi.org/10.1093/jb/mvaa056
Lu, Y. C., Weng, W. C., & Lee, H. (2015). Functional roles of calreticulin in cancer biology. BioMed Research International, 2015, 526524. https://doi.org/10.1155/2015/526524
Ma, Y., Adjemian, S., Mattarollo, S. R., Yamazaki, T., Aymeric, L., Yang, H., . . . Kroemer, G. (2013). Anticancer chemotherapy-induced intratumoral recruitment and differentiation of antigen-presenting cells. Immunity, 38(4), 729-741. https://doi.org/10.1016/j.immuni.2013.03.003
Manoka, S., Sungthong, B., Sato, H., Sugiyama, E., & Sato, V. H. (2016). Hypoglycemic and Antioxidant Activities of the Water Extract of Aquilaria crassna Leaves in Streptozotocin-Nicotinamide-Induced Type-2 Diabetic Mice. Natural Product Communications, 11(6), 757-761.
Muschen, M., Moers, C., Warskulat, U., Niederacher, D., Betz, B., Even, J., . . . Haussinger, D. (1999). CD95 ligand expression in dedifferentiated breast cancer. Journal of Pathology, 189(3), 378-386. https://doi.org/10.1186/bcr405
Neefjes, J., Jongsma, M. L., Paul, P., & Bakke, O. (2011). Towards a systems understanding of MHC class I and MHC class II antigen presentation. Nature Reviews Immunology, 11(12), 823-836. https://doi.org/10.1038/nri3084
Panaretakis, T., Kepp, O., Brockmeier, U., Tesniere, A., Bjorklund, A. C., Chapman, D. C., . . . Kroemer, G. (2009). Mechanisms of pre-apoptotic calreticulin exposure in immunogenic cell death. The EMBO Journal, 28(5), 578-590. https://doi.org/10.1038/emboj.2009.1
Peter, M. E., Hadji, A., Murmann, A. E., Brockway, S., Putzbach, W., Pattanayak, A., & Ceppi, P. (2015). The role of CD95 and CD95 ligand in cancer. Cell death and Differentiation, 22(4), 549-559. https://doi.org/10.1038/cdd.2015.3
Quan, X., Kwak, B. S., Lee, J.-Y., Park, J. H., Lee, A., Kim, T. H., & Park, S. G. (2020). Cordyceps militaris Induces Immunogenic Cell Death and Enhances Antitumor Immunogenic Response in Breast Cancer. Evidence-Based Complementary and Alternative Medicine, 2020, 1-11. https://doi.org/10.1155/2020/9053274
Song, J., Li, J., Hou, F., Wang, X., & Liu, B. (2015). Mangiferin inhibits endoplasmic reticulum stress-associated thioredoxin-interacting protein/NLRP3 inflammasome activation with regulation of AMPK in endothelial cells. Metabolism, 64(3), 428-437. https://doi.org/10.1016/j.metabol.2014.11.008
Supasuteekul, C., Tadtong, S., Putalun, W., Tanaka, H., Likhitwitayawuid, K., Tengamnuay, P., Sritularak, B. (2017). Neuritogenic and neuroprotective constituents from Aquilaria crassna leaves. Journal of Food Biochemistry, 41, e12365.
Suvitayavat, W., Tunglert, S., Thirawarapan, S. S., & Bunyapraphatsara, N. (2005). Effects of Ya-hom on blood pressure in rats. Journal of Ethnopharmacology, 97(3), 503-508. https://doi.org/10.1016/j.jep.2004.12.004
Tan, P. H., Ellis, I., Allison, K., Brogi, E., Fox, S. B., Lakhani, S., . . . Cree, I. A. (2020). The 2019 World Health Organization classification of tumours of the breast. Histopathology, 77(2), 181-185. https://doi.org/10.1111/his.14091
Torigoe, T., Asanuma, H., Nakazawa, E., Tamura, Y., Hirohashi, Y., Yamamoto, E., . . . Sato, N. (2012). Establishment of a monoclonal anti-pan HLA class I antibody suitable for immunostaining of formalin-fixed tissue: unusually high frequency of down-regulation in breast cancer tissues. Pathology International, 62(5), 303-308. https://doi.org/10.1111/j.1440-1827.2012.02789.x
Webb, M. J., & Kukard, C. (2020). A Review of Natural Therapies Potentially Relevant in Triple Negative Breast Cancer Aimed at Targeting Cancer Cell Vulnerabilities. Integrative Cancer Therapies, 19, 1534735420975861. https://doi.org/10.1177/1534735420975861
Wisutthathum, S., Kamkaew, N., Inchan, A., Chatturong, U., Paracha, T. U., Ingkaninan, K., . . . Chootip, K. (2019). Extract of Aquilaria crassna leaves and mangiferin are vasodilators while showing no cytotoxicity. Journal of Traditional and Complementary Medicine, 9(4), 237-242. https://doi.org/10.1016/j.jtcme.2018.09.002
Wongwad, E., Ingkaninan, K., Wisuitiprot, W., Sritularak, B., & Waranuch, N. (2020). Thermal Degradation Kinetics and pH-Rate Profiles of Iriflophenone 3,5-C-beta-d-diglucoside, Iriflophenone 3-C-beta-d-Glucoside and Mangiferin in Aquilaria crassna Leaf Extract. Molecules, 25(21), 4898. https://doi.org/10.3390/molecules25214898
Wongwad, E., Pingyod, C., Saesong, T., Waranuch, N., Wisuitiprot, W., Sritularak, B., . . . Ingkaninan, K. (2019). Assessment of the bioactive components, antioxidant, antiglycation and anti-inflammatory properties of Aquilaria crassna Pierre ex Lecomte leaves. Industrial Crops and Products, 138, 111448. https://doi.org/10.1016/j.indcrop.2019.06.011
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