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Molecules
2019 Aug 29;2417:. doi: 10.3390/molecules24173154.
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Effects of Polar Steroids from the Starfish Patiria (=Asterina) pectinifera in Combination with X-Ray Radiation on Colony Formation and Apoptosis Induction of Human Colorectal Carcinoma Cells.
Malyarenko OS
,
Malyarenko TV
,
Kicha AA
,
Ivanchina NV
,
Ermakova SP
.
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Despite significant advances in the understanding, prevention, and treatment of cancer, the disease continues to affect millions of people worldwide. Chemoradiation therapy is a rational approach that has already proven beneficial for several malignancies. However, the existence of toxicity to normal tissue is a serious limitation of this treatment modality. The aim of the present study is to investigate the ability of polar steroids from starfish Patiria (=Asterina) pectinifera to enhance the efficacy of radiation therapy in colorectal carcinoma cells. The cytotoxic activity of polar steroids and X-ray radiation against DLD-1, HCT 116, and HT-29 cells was determined by an MTS assay. The effect of compounds, X-ray, and their combination on colony formation was studied using the soft agar method. The molecular mechanism of the radiosensitizing activity of asterosaponin P1 was elucidated by western blotting and the DNA comet assay. Polar steroids inhibited colony formation in the tested cells, and to a greater extent in HT-29 cells. Asterosaponin P1 enhanced the efficacy of radiation and, as a result, reduced the number and size of the colonies of colorectal cancer cells. The radiosensitizing activity of asterosaponin P1 was realized by apoptosis induction through the regulation of anti- and pro-apoptotic protein expression followed by caspase activation and DNA degradation.
Figure 1. The structure of polar steroids isolated from starfish P. pectinifera.
Figure 2. The effect of polar steroids from P. pectinifera (1â3) and X-ray radiation on colony formation in human colorectal carcinoma cells. DLD-1 (A), HCT 116 (B), and HT-29 (C) cells (2.4 à 104) with or without polar steroid 1â3 (40 µM) or (D,E) X-ray radiation (2â10 Gy) treatment were subcultured onto 0.3% Basal Medium Eagle (BME) agar containing 10% FBS, 2 mM L-glutamine, and 25 µg/mL gentamicin. After 14 days of incubation, the number (AâD) and size (E) of the colonies were evaluated under a microscope with the aid of the ImageJ software program. All experiments were repeated at least three times in each group (n = 9 for control or compounds treated cells or X-ray exposed cells, nâquantity of photos). Results are expressed as the mean ± standard deviation (SD). The asterisk (*) indicates a significant decrease in the number or size of the colonies of cancer cells treated by polar steroids or X-ray compared to PBS-treated cells (*p < 0.05, **p < 0.01, ***p < 0.001).
Figure 3. The radiosensitizing effects of polar steroids from P. pectinifera (1â3) on colony formation in human colorectal carcinoma cells. DLD-1 (A,B), HCT 116 (C,D), and HT-29 (E,F) cells (2.4 à 104) were either treated or not treated with a combination of polar steroids 1â3 (1, 2, 4 µM) and X-ray radiation (2 Gy) and subcultured onto 0.3% Basal Medium Eagle (BME) agar containing 10% FBS, 2 mM L-glutamine, and 25 µg/mL gentamicin. After 14 days of incubation, the number (A,C,E) and size (B,D,F) of the colonies was evaluated under a microscope with the aid of the ImageJ software program. All experiments were repeated at least three times in each group (n = 9 for control or compounds treated cells or X-ray exposed cells, nâquantity of photos). The magnification of representative photos is 10Ã. Results are expressed as the mean ± standard deviation (SD). The asterisk (*) indicates a significant decrease in the number or size of colonies of cancer cells treated with X-ray compared to PBS-treated cells or polar steroids in combination with X-ray compared to irradiated cells (*p < 0.05, ***p < 0.001).
Figure 4. The effect of combinatorial treatment by asterosaponin P1 from P. pectinifera with radiation on apoptosis induction in HT-29 cells. (A) Regulation of the anti-apoptotic (Bcl-XL) and pro-apoptotic (Bax) proteins expression as well as the initiator (caspase 9) and effector (caspase 3, cleaved caspase 3) caspases, and b-actin by X-ray or with a combination of asterosaponin P1 and X-ray in HT-29 cells. (B) Relative bands density was measured using Image Lab⢠Software 4.1. Quantitative results are presented as the mean values from three independent experiments. Significant differences were evaluated using the Studentâs t-test. The asterisks (***p < 0.001) indicate a significant alteration of protein expression in cells treated by X-ray compared to PBS-treated cells, or asterosaponin P1 in combination with X-ray compared to irradiated cells. (C) HT-29 cells were either treated or not treated by X-ray (2 Gy) or with a combination of asterosaponin P1 (4 µM) and radiation (2 Gy). DNA comets were stained with ethidium bromide and visualized using a fluorescent microscope ZOE⢠Fluorescent Cell Imager. Representative images (Scale bar = 100 µm).
Belka,
Apoptosis-modulating agents in combination with radiotherapy-current status and outlook.
2004, Pubmed
Belka,
Apoptosis-modulating agents in combination with radiotherapy-current status and outlook.
2004,
Pubmed
Blumenthal,
Methods and goals for the use of in vitro and in vivo chemosensitivity testing.
2007,
Pubmed
Bray,
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
2018,
Pubmed
Chen,
Improving radiotherapy in cancer treatment: Promises and challenges.
2017,
Pubmed
Collins,
The comet assay for DNA damage and repair: principles, applications, and limitations.
2004,
Pubmed
Dong,
Chemical constituents and bioactivities of starfish.
2011,
Pubmed
,
Echinobase
Green,
Just So Stories about the Evolution of Apoptosis.
2016,
Pubmed
Ha,
Asterosaponins from the tropical starfish Acanthaster planci and their cytotoxic and anticancer activities in vitro.
2021,
Pubmed
,
Echinobase
Häfner,
Radiotherapy for Colorectal Cancer: Current Standards and Future Perspectives.
2016,
Pubmed
Higuchi,
Biologically active glycosides from asteroidea, 42. Isolation and structure of a new biologically active ganglioside molecular species from the starfish Asterina pectinifera.
2006,
Pubmed
,
Echinobase
Jin,
Overview of cell death signaling pathways.
2005,
Pubmed
Kicha,
The distribution of free sterols, polyhydroxysteroids and steroid glycosides in various body components of the starfish Patiria (=Asterina) pectinifera.
2001,
Pubmed
,
Echinobase
Kim,
Therapeutic Implications for Overcoming Radiation Resistance in Cancer Therapy.
2015,
Pubmed
Lu,
Cytotoxic Polyhydroxysteroidal Glycosides from Starfish Culcita novaeguineae.
2018,
Pubmed
,
Echinobase
Malyarenko,
The Inhibitory Activity of Luzonicosides from the Starfish Echinaster luzonicus against Human Melanoma Cells.
2017,
Pubmed
,
Echinobase
Malyarenko,
Radiosensitizing effect of the fucoidan from brown alga Fucus evanescens and its derivative in human cancer cells.
2019,
Pubmed
Malyarenko,
In Vitro Anticancer and Proapoptotic Activities of Steroidal Glycosides from the Starfish Anthenea aspera.
2018,
Pubmed
,
Echinobase
Mishra,
Prospective of colon cancer treatments and scope for combinatorial approach to enhanced cancer cell apoptosis.
2013,
Pubmed
Nambiar,
Effects of phytochemicals on ionization radiation-mediated carcinogenesis and cancer therapy.
2011,
Pubmed
Nandhakumar,
Evaluation of DNA damage using single-cell gel electrophoresis (Comet Assay).
2011,
Pubmed
Olive,
Heterogeneity in radiation-induced DNA damage and repair in tumor and normal cells measured using the "comet" assay.
1990,
Pubmed
Pal'yanova,
Neurotrophic effects of polyhydroxylated steroids and steroid glycosides in cultured neuroblastoma cells.
2006,
Pubmed
,
Echinobase
Palyanova,
Neuritogenic and neuroprotective effects of polar steroids from the Far East starfishes Patiria pectinifera and Distolasterias nipon.
2013,
Pubmed
,
Echinobase
Peng,
Polyhydroxy steroids and saponins from China Sea starfish Asterina pectinifera and their biological activities.
2010,
Pubmed
,
Echinobase
Tait,
Mitochondria and cell death: outer membrane permeabilization and beyond.
2010,
Pubmed
Tang,
Cytotoxic asterosaponins capable of promoting polymerization of tubulin from the starfish Culcita novaeguineae.
2009,
Pubmed
,
Echinobase
Vien,
Steroid glycosides from the starfish Pentaceraster gracilis.
2017,
Pubmed
,
Echinobase
Yue,
Natural Products as Adjunctive Treatment for Pancreatic Cancer: Recent Trends and Advancements.
2017,
Pubmed
Zhang,
Natural Product Interventions for Chemotherapy and Radiotherapy-Induced Side Effects.
2018,
Pubmed
Zhao,
Asterosaponin 1 induces endoplasmic reticulum stress-associated apoptosis in A549 human lung cancer cells.
2011,
Pubmed
,
Echinobase
Zhou,
Novaeguinoside II inhibits cell proliferation and induces apoptosis of human brain glioblastoma U87MG cells through the mitochondrial pathway.
2011,
Pubmed
,
Echinobase