Curcumin-gold nanoshell mediated near-infrared irradiation on human ovarian cancer cell: in vitro study

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Curcumin-gold nanoshells combined with near-infrared irradiation significantly reduced ovarian cancer cell viability by inducing apoptosis, decreasing HSPB1 expression and altering Bax/Bcl2 ratios.

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This in vitro study synthesized curcumin-conjugated silica-gold nanoshells (Cur-AuNShs) and characterized them by UV–VIS spectroscopy, TEM, DLS, and zeta potential, then tested their effects on human ovarian carcinoma SKOV-3 cells. Cells were exposed to Cur (15 μM) plus AuNShs (75 μM) with near-infrared laser irradiation (2.5 W/cm³) for 5 or 10 minutes, and viability was measured at 48 hours by MTT; apoptosis-related gene expression was assessed by real-time PCR for Bax, Bcl2, and HSPB1. After Cur-AuNShs plus 10 minutes of laser treatment, cell viability decreased significantly (reported from 44.3 ± 1.7 to 14.4 ± 1), with increased Bax and decreased Bcl2, while HSPB1 expression was reduced in the laser-treated group. The paper explicitly reports that no datasets were generated or analyzed and does not include in vivo validation. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Ovarian cancer is considered a predominant female reproductive malignancy and poses a significant threat due to its 80-90% fatality rate. The typical approach involves surgery and chemotherapy, which due to problems such as drug resistance, encourage researchers to use new methods such as nanotechnology. The current study introduces a novel strategy: leveraging Curcumin-Gold Nanoshells (Cur-AuNShs) to combat chemotherapy's adverse effects and overcome drug resistance through hyperthermia mediation. Gold-based nanoparticles that absorb laser have shown the potential to target and treat cancer selectively through highly efficient light-to-heat conversion. This experimental study focused on the synthesis of AuNShs and their subsequent conjugation with Cur. The gold shell coverage on the surfaces of silica nanoparticles was examined using UV-VIS spectroscopy and transmission electron microscopy (TEM). Dynamic light scattering (DLS) and Zeta potential analysis were employed to evaluate the stability of particle size and surface charge. Human ovarian carcinoma cell lines (SKOV-3) were treated with a combination of Cur (15 μM) and AuNShs (75 μM), under the activation of near-infrared (NIR) laser irradiation at a power of 2.5 W/cm3 for 5 or 10 min. Cell viability was then assessed using the MTT assay. Lastly, the expression levels of Bax, Bcl2, and HSPB1 genes were analyzed using the real-time polymerase chain reaction (real-time PCR) technique. The average diameter of the AuNShs was measured at 70 ± 7.1 nm. Findings revealed that after a 48 h incubation with Cur-AuNShs followed by 10 min of laser irradiation, cell viability decreased significantly from 44.3 ± 1.7 to 14.4 ± 1. Analysis using real-time PCR showed an increase in Bax expression alongside a decrease in Bcl2 expression. Additionally, the expression of the HSPB1 gene was reduced from 1.35 ± 1 to 0.9 ± 0.65 in the laser-treated Cur-AuNShs-NIR group. The AuNShs, when combined with hyperthermia at 43 °C, demonstrated potential as an effective carrier for Cur administration. This combination was associated with a greater activation of apoptosis compared to the free drug.
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Abstract

Ovarian cancer is considered a predominant female reproductive malignancy and poses a significant threat due to its 80–90% fatality rate. The typical approach involves surgery and chemotherapy, which due to problems such as drug resistance, encourage researchers to use new methods such as nanotechnology. The current study introduces a novel strategy: leveraging Curcumin-Gold Nanoshells (Cur-AuNShs) to combat chemotherapy’s adverse effects and overcome drug resistance through hyperthermia mediation. Gold-based nanoparticles that absorb laser have shown the potential to target and treat cancer selectively through highly efficient light-to-heat conversion. This experimental study focused on the synthesis of AuNShs and their subsequent conjugation with Cur. The gold shell coverage on the surfaces of silica nanoparticles was examined using UV–VIS spectroscopy and transmission electron microscopy (TEM). Dynamic light scattering (DLS) and Zeta potential analysis were employed to evaluate the stability of particle size and surface charge. Human ovarian carcinoma cell lines (SKOV-3) were treated with a combination of Cur (15 μM) and AuNShs (75 μM), under the activation of near-infrared (NIR) laser irradiation at a power of 2.5 W/cm3 for 5 or 10 min. Cell viability was then assessed using the MTT assay. Lastly, the expression levels of Bax, Bcl2, and HSPB1 genes were analyzed using the real-time polymerase chain reaction (real-time PCR) technique. The average diameter of the AuNShs was measured at 70 ± 7.1 nm. Findings revealed that after a 48 h incubation with Cur-AuNShs followed by 10 min of laser irradiation, cell viability decreased significantly from 44.3 ± 1.7 to 14.4 ± 1. Analysis using real-time PCR showed an increase in Bax expression alongside a decrease in Bcl2 expression. Additionally, the expression of the HSPB1 gene was reduced from 1.35 ± 1 to 0.9 ± 0.65 in the laser-treated Cur-AuNShs-NIR group. The AuNShs, when combined with hyperthermia at 43 °C, demonstrated potential as an effective carrier for Cur administration. This combination was associated with a greater activation of apoptosis compared to the free drug. Similar content being viewed by others Data availability No datasets were generated or analyzed during the current study.

References

Ames B, Gold L, editors. Natural chemicals, synthetic chemicals, risk assessment, and cancer. Princess Takamatsu symposia; 1990. Khan S. Potential role of Escherichia coli DNA mismatch repair proteins in colon cancer. Crit Rev Oncol Hematol. 2015;96(3):475–82. Khan S, Mosvi SN, Vohra S, Poddar NK. Implication of calcium supplementations in health and diseases with special focus on colorectal cancer. Crit Rev Clin Lab Sci. 2024;61(6):496–509. Khan S, Zakariah M, Rolfo C, Robrecht L, Palaniappan S. Prediction of mycoplasma hominis proteins targeting in mitochondria and cytoplasm of host cells and their implication in prostate cancer etiology. Oncotarget. 2016;8(19):30830. Khan S, Zakariah M, Palaniappan S. Computational prediction of Mycoplasma hominis proteins targeting in nucleus of host cell and their implication in prostate cancer etiology. Tumor Biol. 2016;37:10805–13. Khan S, Imran A, Khan AA, Abul Kalam M, Alshamsan A. Systems biology approaches for the prediction of possible role of Chlamydia pneumoniae proteins in the etiology of lung cancer. PLoS ONE. 2016;11(2): e0148530. Wang Y, Imran A, Shami A, Chaudhary AA, Khan S. Decipher the Helicobacter pylori protein targeting in the nucleus of host cell and their implications in gallbladder cancer: an insilico approach. J Cancer. 2021;12(23):7214. Khan S, Zaidi S, Alouffi AS, Hassan I, Imran A, Khan RA. Computational proteome-wide study for the prediction of Escherichia coli protein targeting in host cell organelles and their implication in development of colon cancer. ACS Omega. 2020;5(13):7254–61. Reid BM, Permuth JB, Sellers TAJCb. Epidemiology of ovarian cancer: a review. Cancer Biol Med. 2017;14(1):9. Vallius T, Hynninen J, Kemppainen J, Alves V, Auranen K, Matomäki J, et al. 18 F-FDG-PET/CT based total metabolic tumor volume change during neoadjuvant chemotherapy predicts outcome in advanced epithelial ovarian cancer. Eur J Nucl Med Mol Imaging. 2018;45:1224–32. Zielińska A, Alves H, Marques V, Durazzo A, Lucarini M, Alves TF, et al. Properties, extraction methods, and delivery systems for curcumin as a natural source of beneficial health effects. Medicina. 2020;56(7):336. Weir NM, Selvendiran K, Kutala VK, Tong L, Vishwanath S, Rajaram M, et al. Curcumin induces G2/M arrest and apoptosis in cisplatin-resistant human ovarian cancer cells by modulating akt and p38 mAPK. Cancer Biol Ther. 2007;6(2):178–84. Lu H-F, Lai K-C, Hsu S-C, Lin H-J, Yang M-D, Chen Y-L, et al. Curcumin induces apoptosis through FAS and FADD, in caspase-3-dependent and-independent pathways in the N18 mouse-rat hybrid retina ganglion cells. Oncol Rep. 2009;22(1):97–104. Chen X-P, Li Y, Zhang Y, Li G. Formulation, characterization and evaluation of curcumin-loaded PLGA-TPGS nanoparticles for liver cancer treatment. Drug Design Dev Ther. 2019;13:3569–78. Hak A, Shinde VR, Rengan AKJP, Therapy P. A review of advanced nanoformulations in phototherapy for cancer therapeutics. Photodiagn Photodyn Ther. 2021;33: 102205. Malviya N, Malviya S, Saxena R, Chauhan V, Dhere M. Smart biodegradable polymeric nanoparticles: synthesis, characterization, and applications. In: Advancements in controlled drug delivery systems. New York: IGI Global; 2022. p. 257–80. Ombredane AS, Silva VR, Andrade LR, Pinheiro WO, Simonelly M, Oliveira JV, et al. In vivo efficacy and toxicity of curcumin nanoparticles in breast cancer treatment: a systematic review. Front Oncol. 2021;11: 612903. Sun L, Xu H,Xu J-h, Wang S-N, Wang J-W, Zhang H-F, et al. Enhanced antitumor efficacy of curcumin-loaded PLGA nanoparticles coated with unique fungal hydrophobin. AAPS PharmSciTech. 2020;21:1–10. Ipar VS, Dsouza A, Devarajan PVJE. Enhancing curcumin oral bioavailability through nanoformulations. Eur J Drug Metab Pharmacokinet. 2019;44:459–80. Elahi N, Kamali M, Baghersad MHJT. Recent biomedical applications of gold nanoparticles: a review. Talanta. 2018;184:537–56. Nambiar S, Osei E, Fleck A, Darko J, Mutsaers AJ, Wettig SJAN. Synthesis of curcumin-functionalized gold nanoparticles and cytotoxicity studies in human prostate cancer cell line. Appl Nanosci. 2018;8:347–57. Mahmoudi A, Kesharwani P, Majeed M, Teng Y, Sahebkar AJC, Biointerfaces SB. Recent advances in nanogold as a promising nanocarrier for curcumin delivery. Colloids Surf B. 2022;215: 112481. Yan T, Su M, Wang Z, Zhang JJS. Second near-infrared plasmonic nanomaterials for photoacoustic imaging and photothermal therapy. Small. 2023;19(30):2300539. Phuong PTM, Jhon H, In I. Photothermal-modulated reversible volume transition of wireless hydrogels embedded with redox-responsive carbon dots. Biomater Sci. 2019;7(11):4800–12. Riley RS, Day ESJ. Gold nanoparticle-mediated photothermal therapy: applications and opportunities for multimodal cancer treatment. Wiley Interdisc Rev. 2017;9(4): e1449. Ghobashy MM, Alkhursani SA, Alqahtani HA, El-damhougy TK, Madani MJMS. Gold nanoparticles in microelectronics advancements and biomedical applications. Mater Sci Eng. 2024;301:117191. De Matteis V, Cascione M, Toma CC, Rinaldi RJC. Engineered gold nanoshells killing tumor cells: new perspectives. Curr Pharm Design. 2019;25(13):1477–89. Nouri S, Mohammadi E, Mehravi B, Majidi F, Ashtari K, Neshasteh-Riz A, et al. NIR triggered glycosylated gold nanoshell as a photothermal agent on melanoma cancer cells. Artif Cells Nanomed Biotechnol. 2019;47(1):2316–24. Martin RC, Locatelli E, Li Y, Zhang W, Li S, Monaco I, et al. Gold nanorods and curcumin-loaded nanomicelles for efficient in vivo photothermal therapy of Barrett’s esophagus. Nanomedicine. 2015;10(11):1723–33. Kayani Z, Vais RD, Soratijahromi E, Mohammadi S, Sattarahmady NJP, Therapy P. Curcumin-gold-polyethylene glycol nanoparticles as a nanosensitizer for photothermal and sonodynamic therapies: in vitro and animal model studies. Photodiagn Photodyn Ther. 2021;33: 102139. Singh SP, Alvi SB, Pemmaraju DB, Singh AD, Manda SV, Srivastava R, et al. NIR triggered liposome gold nanoparticles entrapping curcumin as in situ adjuvant for photothermal treatment of skin cancer. Int J Biol Microbiol. 2018;110:375–82. Heiserman JP, Nallanthighal S, Gifford CC, Graham K, Samarakoon R, Gao C, et al. Heat shock protein 27, a novel downstream target of collagen type XI alpha 1, synergizes with fatty acid oxidation to confer cisplatin resistance in ovarian cancer cells. Cancers. 2021;13(19):4855. Bilous I, Pavlovych L, Krynytska I, Marushchak M, Kamyshnyi A. Apoptosis and cell cycle pathway-focused genes expression analysis in patients with different forms of thyroid pathology. 2020. Ren G, Su H, Wang SJJ. The combined method to synthesis silica nanoparticle by Stöber process. J Sol-Gel Sci Technol. 2020;96:108–20. García-Soto MJ, González-Ortega OJGB. Synthesis of silica-core gold nanoshells and some modifications/variations. Gold Bull. 2016;49:111–31. Gao Y, Torrente-Murciano LJN. Mechanistic insights of the reduction of gold salts in the Turkevich protocol. Nanoscale. 2020;12(4):2740–51. Oćwieja M, Maciejewska-Prończuk J, Adamczyk Z, Roman MJ. Formation of positively charged gold nanoparticle monolayers on silica sensors. J Colloid Interface Sci. 2017;501:192–201. dos Santos CD, Teixeira BH, Pereira CBP, Franzolin MR. Pegylated curcumin with gold nanoparticles: antimicrobial agent evaluation. J Biomed Eng Biosci. 2016;3(1):43–7. Sharma K, Agrawal S, Gupta MJIJDDR. Development and validation of UV spectrophotometric method for the estimation of curcumin in bulk drug and pharmaceutical dosage forms. Int J Drug Dev Res. 2012;4(2):375–80. Alwattar JK, Mneimneh AT, Abla KK, Mehanna MM, Allam ANJP. Smart stimuli-responsive liposomal nanohybrid systems: a critical review of theranostic behavior in cancer. Pharmaceutics. 2021;13(3):355. Chaichian S, Kashi AM, Tehermanesh K, Mahabadi VP, Minaeian S, Eslahi NJCJ. Effect of PLGA nanoparticle-mediated delivery of MiRNA 503 on the apoptosis of ovarian endometriosis cells. Cell J. 2022;24(11):697. Shanmugam MK, Rane G, Kanchi MM, Arfuso F, Chinnathambi A, Zayed M, et al. The multifaceted role of curcumin in cancer prevention and treatment. Molecules. 2015;20(2):2728–69. Doello K, Ortiz R, Alvarez PJ, Melguizo C, Cabeza L, Prados JJN, et al. Latest in vitro and in vivo assay, clinical trials and patents in cancer treatment using curcumin: a literature review. Nutr Cancer. 2018;70(4):569–78. Rastinehad AR, Anastos H, Wajswol E, Winoker JS, Sfakianos JP, Doppalapudi SK, et al. Gold nanoshell-localized photothermal ablation of prostate tumors in a clinical pilot device study. Proc Natl Acad Sci. 2019;116(37):18590–6. Kong X-X, Jiang S, Liu T, Liu G-F, Dong M. Paclitaxel increases sensitivity of SKOV3 cells to hyperthermia by inhibiting heat shock protein 27. Biomed Pharmacother. 2020;132: 110907. Yu Z, Wan Y, Liu Y, Yang J, Li L, Zhang W. Curcumin induced apoptosis via PI3K/Akt-signalling pathways in SKOV3 cells. Pharm Biol. 2016;54(10):2026–32. Woźniak A, Malankowska A, Nowaczyk G, Grześkowiak BF, Tuśnio K, Słomski R, et al. Size and shape-dependent cytotoxicity profile of gold nanoparticles for biomedical applications. J Mater Sci. 2017;28:1–11. Xia Q, Huang J, Feng Q, Chen X, Liu X, Li X, et al. Size-and cell type-dependent cellular uptake, cytotoxicity and in vivo distribution of gold nanoparticles. Int J Nanomed. 2019;14:6957–70. Rezakhani L, Fekri K, Rostaminasab G, Rahmati SJMO. Exosomes: special nano-therapeutic carrier for cancers, overview on anticancer drugs. Med Oncol. 2022;40(1):31. Piktel E, Ościłowska I, Suprewicz Ł, Depciuch J, Marcińczyk N, Chabielska E, et al. ROS-mediated apoptosis and autophagy in ovarian cancer cells treated with peanut-shaped gold nanoparticles. Int J Nanomed. 2021;16:1993. Alipour S, Babaei G, Aziz SG-G, Abolhasani S. Alantolactone and ZnO nanoparticles induce apoptosis activity of cisplatin in an ovarian cancer cell line (SKOV3). Res Pharm Sci. 2022;17(3):294. Abedi M, Babaei E. Study of the effect of dendrosomal nano-curcumin on expression of apoptotic Bax and Bcl2 genes in cancerous cell line AGS. J Police Med. 2015;3(4):203–10. Chen C-H, Chan T-M, Wu Y-J, Chen J-J. Application of nanoparticles in urothelial cancer of the urinary bladder. J Med Biol Eng. 2015;35:419–27. Rau L-R, Huang W-Y, Liaw J-W, Tsai S-W. Photothermal effects of laser-activated surface plasmonic gold nanoparticles on the apoptosis and osteogenesis of osteoblast-like cells. Int J Nanomed. 2016;11:3461. Liang Z, Li X, Xie Y, Liu S. ‘Smart’gold nanoshells for combined cancer chemotherapy and hyperthermia. Biomed Mater. 2014;9(2): 025012. Lee S-Y, Shieh M-J. Platinum (II) drug-loaded gold nanoshells for chemo-photothermal therapy in colorectal cancer. ACS Appl Mater Interfaces. 2020;12(4):4254–64. Yang S-J, Pai J-A, Shieh M-J, Chen JLY, Chen K-C. Cisplatin-loaded gold nanoshells mediate chemo-photothermal therapy against primary and distal lung cancers growth. Biomed Pharmacother. 2023;158: 114146. Emamzadeh M, Pasparakis G. Polymer coated gold nanoshells for combinational photochemotherapy of pancreatic cancer with gemcitabine. Sci Rep. 2021;11(1):9404. Pourgholi A, Dadashpour M, Mousapour A, Amandi AF, Zarghami N. Anticancer potential of silibinin loaded polymeric nanoparticles against breast cancer cells: insight into the apoptotic genes targets. Asian Pac J Cancer Prev. 2021;22(8):2587. Hassani N, Jafari-Gharabaghlou D, Dadashpour M, Zarghami N. The effect of dual bioactive compounds artemisinin and metformin co-loaded in PLGA-PEG nano-particles on breast cancer cell lines: potential apoptotic and anti-proliferative action. Appl Biochem Biotechnol. 2022;194(10):4930–45. Azar LK, Dadashpour M, Hashemi M, Zarghami N. Design and development of nanostructured co delivery of artemisinin and chrysin for targeting hTERT gene expression in breast cancer cell line: possible clinical application in cancer treatment. Asian Pac J Cancer Prev. 2022;23(3):919. Wang H-X, Yang Y, Guo H, Hou D-D, Zheng S, Hong Y-X, et al. HSPB1 deficiency sensitizes melanoma cells to hyperthermia induced cell death. Oncotarget. 2016;7(41):67449.

Acknowledgements

This study was funded by a grant from Iran University of Medical Sciences (IUMS). We would like to give great thanks to the Nanotechnology Department of Iran University of Medical Sciences. Funding This study was funded by a grant from Iran University of Medical Sciences (IUMS). Author information Authors and Affiliations Contributions All the authors contributed to the preparation of the manuscript. Corresponding authors Ethics declarations Conflict of interest The authors declare that there is no conflict of interest in this study. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Rokhgireh, S., Chaichian, S., Mehdizadeh Kashi, A. et al. Curcumin-gold nanoshell mediated near-infrared irradiation on human ovarian cancer cell: in vitro study. Med Oncol 42, 145 (2025). https://doi.org/10.1007/s12032-025-02687-4 Received: Accepted: Published: Version of record: DOI: https://doi.org/10.1007/s12032-025-02687-4

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Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Antineoplastic Agents Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin Curcumin

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