Chrysin and chrysin-loaded nanocarriers induced immunogenic cell death on B16 melanoma cells

被引:0
|
作者
Yasaman Oliyapour
Sheida Dabiri
Ommoleila Molavi
Mohammad Saeid Hejazi
Soodabeh Davaran
Sevda Jafari
Soheila Montazersaheb
机构
[1] Tabriz University of Medical Sciences,Department of Pharmaceutical Biotechnology, Faculty of Pharmacy
[2] Tabriz University of Medical Science,Biotechnology Research Center
[3] Tabriz University of Medical Sciences,Molecular Medicine Research Center
[4] Tabriz University of Medical Sciences,Department of Pharmaceutical Chemistry, Faculty of Pharmacy
[5] Tabriz University of Medical Sciences,Nutrition Research Center
来源
关键词
Chrysin; Nanocarriers; Immunogenic cell death; Cancer; Endoplasmic reticulum;
D O I
暂无
中图分类号
学科分类号
摘要
Induction of immunogenic cell death (ICD) is a promising strategy for cancer immunotherapy. Chrysin, which has potential anticancer effects, faces limitations in clinical applications due to its poor water solubility. This study aimed to formulate chrysin with PEG-poly(α-benzylcarboxylate-ε-caprolactone) (PBCL) nanoparticles (NPs) and assess their anticancer and ICD-inducing potency in melanoma cells, comparing with free chrysin. The co-solvent evaporation method was employed to develop chrysin-loaded NPs. UV spectroscopy, dynamic light scattering, and the dialysis bag method were used to evaluate the encapsulation efficiency (EE), particle size, polydispersity index (PDI), and drug release profile, respectively. The anticancer effects of the drugs were assessed using the MTT and trypan blue exclusion assays. Flow cytometry was employed to evaluate apoptosis and calreticulin (CRT) expression. ELISA and western blotting were used to detect heat shock protein 90 (HSP90), Annexin A1, GRP78 (Glucose-related protein78), and activated protein kinase R-like endoplasmic reticulum kinase (p-PERK). Chrysin-loaded PEG-PBCL NPs (chrysin-PEG-PBCL) showed an EE of 97 ± 1%. Chrysin-PEG-PBCL was 38.18 ± 3.96 nm in size, with a PDI being 0.62 ± 0.23. Chrysin-PEG-PBCL showed an initial burst release, followed by sustained release over 24 h. Chrysin-PEG-PBCL exhibited a significantly stronger anticancer effect in B16 cells. Chrysin-PEG-PBCL was found to be more potent in inducing apoptosis. Both free chrysin and chrysin NPs induced ICD as indicated by an increase in the levels of ICD biomarkers. Interestingly, chrysin NPs were found to be more potent inducers of ICD than the free drug. These findings demonstrate that chrysin and chrysin-PEG-PBCL NPs can induce ICD in B16 cells. PEG-PBCL NPs significantly enhanced the potency of chrysin in inducing ICD compared to its free form.
引用
收藏
相关论文
共 50 条
  • [41] Determination of cell cycle phases in live B16 melanoma cells using IRMS
    Bedolla, Diana E.
    Kenig, Sasa
    Mitri, Elisa
    Ferraris, Paolo
    Marcello, Alessandro
    Grenci, Gianluca
    Vaccari, Lisa
    ANALYST, 2013, 138 (14) : 4015 - 4021
  • [42] Radioresistance mechanisms of side population cells in mouse melanoma cell line B16
    Matchuk O.N.
    Zamulaeva I.A.
    Kovalev O.A.
    Saenko A.S.
    Cell and Tissue Biology, 2013, 7 (6) : 556 - 562
  • [43] Cidofovir inhibits growth of B16 melanoma cells in vivo
    Redondo, P
    Idoate, M
    Galofré, JC
    Solano, T
    BRITISH JOURNAL OF DERMATOLOGY, 2000, 143 (04) : 741 - 748
  • [44] Effect of Chlorogenic Acid on Melanogenesis of B16 Melanoma Cells
    Li, Hao-Rong
    Habasi, Maidina
    Xie, Lian-Zhen
    Aisa, Haji Akber
    MOLECULES, 2014, 19 (09) : 12940 - 12948
  • [45] Involvement of calpain in melanogenesis of mouse B16 melanoma cells
    Ohguchi, K
    Akao, Y
    Nozawa, Y
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2005, 275 (1-2) : 103 - 107
  • [46] Blue light inhibits the growth of B16 melanoma cells
    Ohara, M
    Kawashima, Y
    Katoh, O
    Watanabe, H
    JAPANESE JOURNAL OF CANCER RESEARCH, 2002, 93 (05): : 551 - 558
  • [47] Mechanism of Pigmentation by Minocycline in Murine B16 Melanoma Cells
    Sato, Emi
    Tsukimoto, Mitsutoshi
    Shimura, Noriko
    Awaya, Akira
    Kojima, Shuji
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2011, 131 (05): : 731 - 738
  • [48] Implication of the glutathione on B16 melanoma cells sensitivity to cyclophosphamide
    Bilbao, P
    Palomares, T
    AlonsoVarona, A
    Alvarez, A
    Martin, JC
    Negueruela, JT
    EUROPEAN JOURNAL OF CANCER, 1995, 31A : A220 - A220
  • [49] Involvement of calpain in melanogenesis of mouse B16 melanoma cells
    Kenji Ohguchi
    Yukihiro Akao
    Yoshinori Nozawa
    Molecular and Cellular Biochemistry, 2005, 275 : 103 - 107
  • [50] Cell killing of melanoma B16 in vivo by hyperthermia and cytotoxins
    Stojkovic, R
    Radacic, M
    INTERNATIONAL JOURNAL OF HYPERTHERMIA, 2002, 18 (01) : 62 - 71