Review




Structured Review

Olon Ricerca Bioscience human sw48 colon cancer cell line
(A-B) Mice were injected subcutaneously in the right flank with <t>SW48</t> human colon cancer cells, as described in the Materials and Methods. After two weeks (average tumor size 200-300 mm 3 ), mice were treated intraperitoneally with: PBS (phosphate-buffered saline) control, cetuximab, or MM151. The treatment was continued up to 30 weeks after cancer cell injection. Each group consisted of 10 mice. Tumor volumes were measured three times a week. Animals were sacrificed when tumors achieved 2.000 mm 3 in size. Abbreviations: CTR, control; A, median tumor volume (mm 3 ); B, alive mice/total mice; C, number of mice without clinical evidence of progression. (C-D) Mice were monitored for survival until 30 weeks following tumor cell injection. Differences in animal survival among groups were evaluated by use of the Mantel Cox logrank test. Cetuximab versus CTR, MM151 versus CTR, MM151 versus cetuximab (*** p < 0.05).
Human Sw48 Colon Cancer Cell Line, supplied by Olon Ricerca Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+sw48+colon+cancer+cell/human+sw48+dimethylsulfoxide+cell+line/pmc05669927-100-1-31
Average 90 stars, based on 1 article reviews
human sw48 colon cancer cell line - by Bioz Stars, 2026-09
90/100 stars

Images

1) Product Images from "Antitumor efficacy of triple monoclonal antibody inhibition of epidermal growth factor receptor (EGFR) with MM151 in EGFR-dependent and in cetuximab-resistant human colorectal cancer cells"

Article Title: Antitumor efficacy of triple monoclonal antibody inhibition of epidermal growth factor receptor (EGFR) with MM151 in EGFR-dependent and in cetuximab-resistant human colorectal cancer cells

Journal: Oncotarget

doi: 10.18632/oncotarget.19797

(A-B) Mice were injected subcutaneously in the right flank with SW48 human colon cancer cells, as described in the Materials and Methods. After two weeks (average tumor size 200-300 mm 3 ), mice were treated intraperitoneally with: PBS (phosphate-buffered saline) control, cetuximab, or MM151. The treatment was continued up to 30 weeks after cancer cell injection. Each group consisted of 10 mice. Tumor volumes were measured three times a week. Animals were sacrificed when tumors achieved 2.000 mm 3 in size. Abbreviations: CTR, control; A, median tumor volume (mm 3 ); B, alive mice/total mice; C, number of mice without clinical evidence of progression. (C-D) Mice were monitored for survival until 30 weeks following tumor cell injection. Differences in animal survival among groups were evaluated by use of the Mantel Cox logrank test. Cetuximab versus CTR, MM151 versus CTR, MM151 versus cetuximab (*** p < 0.05).
Figure Legend Snippet: (A-B) Mice were injected subcutaneously in the right flank with SW48 human colon cancer cells, as described in the Materials and Methods. After two weeks (average tumor size 200-300 mm 3 ), mice were treated intraperitoneally with: PBS (phosphate-buffered saline) control, cetuximab, or MM151. The treatment was continued up to 30 weeks after cancer cell injection. Each group consisted of 10 mice. Tumor volumes were measured three times a week. Animals were sacrificed when tumors achieved 2.000 mm 3 in size. Abbreviations: CTR, control; A, median tumor volume (mm 3 ); B, alive mice/total mice; C, number of mice without clinical evidence of progression. (C-D) Mice were monitored for survival until 30 weeks following tumor cell injection. Differences in animal survival among groups were evaluated by use of the Mantel Cox logrank test. Cetuximab versus CTR, MM151 versus CTR, MM151 versus cetuximab (*** p < 0.05).

Techniques Used: Injection, Saline, Control

(A-C) SW48, LIM1215 or CACO2 human colon cancer cells were injected subcutaneously into the right flank of seven nude mice, respectively. After two weeks mice were treated with cetuximab (25 mg/Kg once a week) by i.p. injection. Treatment was continued until disease progression. The black arrows indicate the time of progression to cetuximab. At progression mice were treated with MM151 (25 mg/Kg once a week) by i.p. injection. The treatment was continued until 30 weeks following tumor cell injection. At week 30, five out of seven mice were still on treatment with MM151 in the SW48 and LIM1215 xenograft groups as well as four out of seven in the CACO2 xenograft group (as indicated by double asterisk). Abbreviations: PD, progression disease; PR, partial response; SD, stable disease; wks, weeks.
Figure Legend Snippet: (A-C) SW48, LIM1215 or CACO2 human colon cancer cells were injected subcutaneously into the right flank of seven nude mice, respectively. After two weeks mice were treated with cetuximab (25 mg/Kg once a week) by i.p. injection. Treatment was continued until disease progression. The black arrows indicate the time of progression to cetuximab. At progression mice were treated with MM151 (25 mg/Kg once a week) by i.p. injection. The treatment was continued until 30 weeks following tumor cell injection. At week 30, five out of seven mice were still on treatment with MM151 in the SW48 and LIM1215 xenograft groups as well as four out of seven in the CACO2 xenograft group (as indicated by double asterisk). Abbreviations: PD, progression disease; PR, partial response; SD, stable disease; wks, weeks.

Techniques Used: Injection, Biomarker Discovery

(A-C) Tumors were collected at the beginning of cetuximab treatment and at the onset of resistance to cetuximab from mice engrafted with the SW48, LIM1215 and CACO2 cell lines. As control we used one mouse that has not undergone to any type of treatment from the first in vivo experiment. Tumour samples were collected and total cell protein extracts were subjected to immunoblotting with the indicated antibodies, as described in Materials and Methods. Anti-tubulin antibody was used for normalization of protein extract content.
Figure Legend Snippet: (A-C) Tumors were collected at the beginning of cetuximab treatment and at the onset of resistance to cetuximab from mice engrafted with the SW48, LIM1215 and CACO2 cell lines. As control we used one mouse that has not undergone to any type of treatment from the first in vivo experiment. Tumour samples were collected and total cell protein extracts were subjected to immunoblotting with the indicated antibodies, as described in Materials and Methods. Anti-tubulin antibody was used for normalization of protein extract content.

Techniques Used: Control, In Vivo, Western Blot

Related Articles

Staining:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Microscopy:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Standard Deviation:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Fluorescence:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Control:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Positive Control:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Flow Cytometry:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Incubation:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Expressing:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T

Western Blot:

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer
Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy. .. T



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Olon Ricerca Bioscience human sw48 (kras, nras, braf and pik3ca wild type), colon cancer cell line
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Image Search Results


Cancer cell viability after 72 h exposure to various concentrations of EVOO-PEs derived from different cultivars (Oblica-Sea/Oblica, Buža, Bjelica and Žižolera). HeLa cells ( A ); SW48 cells ( B ). Values are the mean ± SD, n = 4. Means labelled by different letters are significantly different (ANOVA test, p ≤ 0.05).

Journal: Antioxidants

Article Title: Biological Activity of Phenolic Compounds in Extra Virgin Olive Oils through Their Phenolic Profile and Their Combination with Anticancer Drugs Observed in Human Cervical Carcinoma and Colon Adenocarcinoma Cells

doi: 10.3390/antiox9050453

Figure Lengend Snippet: Cancer cell viability after 72 h exposure to various concentrations of EVOO-PEs derived from different cultivars (Oblica-Sea/Oblica, Buža, Bjelica and Žižolera). HeLa cells ( A ); SW48 cells ( B ). Values are the mean ± SD, n = 4. Means labelled by different letters are significantly different (ANOVA test, p ≤ 0.05).

Article Snippet: Human colon cancer (SW48) cells were obtained from cell culture bank (ATCC-LGC, Wesel, Germany).

Techniques: Derivative Assay

Biological activity of EVOO-PEs in HeLa and  SW48  cells obtained from different cultivars expressed as IC 65 (in % v/v of EVOO-PE ± SD).

Journal: Antioxidants

Article Title: Biological Activity of Phenolic Compounds in Extra Virgin Olive Oils through Their Phenolic Profile and Their Combination with Anticancer Drugs Observed in Human Cervical Carcinoma and Colon Adenocarcinoma Cells

doi: 10.3390/antiox9050453

Figure Lengend Snippet: Biological activity of EVOO-PEs in HeLa and SW48 cells obtained from different cultivars expressed as IC 65 (in % v/v of EVOO-PE ± SD).

Article Snippet: Human colon cancer (SW48) cells were obtained from cell culture bank (ATCC-LGC, Wesel, Germany).

Techniques: Activity Assay

HeLa and SW48 cells viability after 72 h exposure to various doses of anticancer drugs in post-treatment (6 h after anticancer drugs) with 0.06% ( v/v ) of EVOO-PEs derived from different cultivars (Oblica-Sea/Oblica, Buža, Bjelica and Žižolera). HeLa cells with cDDP and 0.06% ( v / v ) of EVOO-PE ( A ). SW48 cells with cDDP and 0.06% ( v / v ) of EVOO-PE ( B ). HeLa cells with CBP and 0.06% ( v/v ) of EVOO-PE ( C ). Values are the mean ± SD, n = 4. Means labelled by different letters are significantly different (ANOVA test, p ≤ 0.05).

Journal: Antioxidants

Article Title: Biological Activity of Phenolic Compounds in Extra Virgin Olive Oils through Their Phenolic Profile and Their Combination with Anticancer Drugs Observed in Human Cervical Carcinoma and Colon Adenocarcinoma Cells

doi: 10.3390/antiox9050453

Figure Lengend Snippet: HeLa and SW48 cells viability after 72 h exposure to various doses of anticancer drugs in post-treatment (6 h after anticancer drugs) with 0.06% ( v/v ) of EVOO-PEs derived from different cultivars (Oblica-Sea/Oblica, Buža, Bjelica and Žižolera). HeLa cells with cDDP and 0.06% ( v / v ) of EVOO-PE ( A ). SW48 cells with cDDP and 0.06% ( v / v ) of EVOO-PE ( B ). HeLa cells with CBP and 0.06% ( v/v ) of EVOO-PE ( C ). Values are the mean ± SD, n = 4. Means labelled by different letters are significantly different (ANOVA test, p ≤ 0.05).

Article Snippet: Human colon cancer (SW48) cells were obtained from cell culture bank (ATCC-LGC, Wesel, Germany).

Techniques: Derivative Assay

Pearson correlation among the concentrations of different phenolic compounds in EVOO-PEs and their antioxidant and biological activity in HeLa and  SW48  cells.

Journal: Antioxidants

Article Title: Biological Activity of Phenolic Compounds in Extra Virgin Olive Oils through Their Phenolic Profile and Their Combination with Anticancer Drugs Observed in Human Cervical Carcinoma and Colon Adenocarcinoma Cells

doi: 10.3390/antiox9050453

Figure Lengend Snippet: Pearson correlation among the concentrations of different phenolic compounds in EVOO-PEs and their antioxidant and biological activity in HeLa and SW48 cells.

Article Snippet: Human colon cancer (SW48) cells were obtained from cell culture bank (ATCC-LGC, Wesel, Germany).

Techniques: Activity Assay

The score-plot of samples from principal competent analysis (PC1 vs. PC2). (●) HeLa cells with cDDP and 0.06% ( v/v ) of EVOO-PE. (▲) HeLa cells with cDDP and 0.06% ( v/v ) of EVOO-PE. (■) SW48 cells with cDDP and 0.06% ( v/v ) of EVOO-PE.

Journal: Antioxidants

Article Title: Biological Activity of Phenolic Compounds in Extra Virgin Olive Oils through Their Phenolic Profile and Their Combination with Anticancer Drugs Observed in Human Cervical Carcinoma and Colon Adenocarcinoma Cells

doi: 10.3390/antiox9050453

Figure Lengend Snippet: The score-plot of samples from principal competent analysis (PC1 vs. PC2). (●) HeLa cells with cDDP and 0.06% ( v/v ) of EVOO-PE. (▲) HeLa cells with cDDP and 0.06% ( v/v ) of EVOO-PE. (■) SW48 cells with cDDP and 0.06% ( v/v ) of EVOO-PE.

Article Snippet: Human colon cancer (SW48) cells were obtained from cell culture bank (ATCC-LGC, Wesel, Germany).

Techniques:

(A-B) Mice were injected subcutaneously in the right flank with SW48 human colon cancer cells, as described in the Materials and Methods. After two weeks (average tumor size 200-300 mm 3 ), mice were treated intraperitoneally with: PBS (phosphate-buffered saline) control, cetuximab, or MM151. The treatment was continued up to 30 weeks after cancer cell injection. Each group consisted of 10 mice. Tumor volumes were measured three times a week. Animals were sacrificed when tumors achieved 2.000 mm 3 in size. Abbreviations: CTR, control; A, median tumor volume (mm 3 ); B, alive mice/total mice; C, number of mice without clinical evidence of progression. (C-D) Mice were monitored for survival until 30 weeks following tumor cell injection. Differences in animal survival among groups were evaluated by use of the Mantel Cox logrank test. Cetuximab versus CTR, MM151 versus CTR, MM151 versus cetuximab (*** p < 0.05).

Journal: Oncotarget

Article Title: Antitumor efficacy of triple monoclonal antibody inhibition of epidermal growth factor receptor (EGFR) with MM151 in EGFR-dependent and in cetuximab-resistant human colorectal cancer cells

doi: 10.18632/oncotarget.19797

Figure Lengend Snippet: (A-B) Mice were injected subcutaneously in the right flank with SW48 human colon cancer cells, as described in the Materials and Methods. After two weeks (average tumor size 200-300 mm 3 ), mice were treated intraperitoneally with: PBS (phosphate-buffered saline) control, cetuximab, or MM151. The treatment was continued up to 30 weeks after cancer cell injection. Each group consisted of 10 mice. Tumor volumes were measured three times a week. Animals were sacrificed when tumors achieved 2.000 mm 3 in size. Abbreviations: CTR, control; A, median tumor volume (mm 3 ); B, alive mice/total mice; C, number of mice without clinical evidence of progression. (C-D) Mice were monitored for survival until 30 weeks following tumor cell injection. Differences in animal survival among groups were evaluated by use of the Mantel Cox logrank test. Cetuximab versus CTR, MM151 versus CTR, MM151 versus cetuximab (*** p < 0.05).

Article Snippet: The human SW48 (catalogue number: HTL99020) ( KRAS, NRAS, BRAF and PIK3CA wild type) colon cancer cell line was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Injection, Saline, Control

(A-C) SW48, LIM1215 or CACO2 human colon cancer cells were injected subcutaneously into the right flank of seven nude mice, respectively. After two weeks mice were treated with cetuximab (25 mg/Kg once a week) by i.p. injection. Treatment was continued until disease progression. The black arrows indicate the time of progression to cetuximab. At progression mice were treated with MM151 (25 mg/Kg once a week) by i.p. injection. The treatment was continued until 30 weeks following tumor cell injection. At week 30, five out of seven mice were still on treatment with MM151 in the SW48 and LIM1215 xenograft groups as well as four out of seven in the CACO2 xenograft group (as indicated by double asterisk). Abbreviations: PD, progression disease; PR, partial response; SD, stable disease; wks, weeks.

Journal: Oncotarget

Article Title: Antitumor efficacy of triple monoclonal antibody inhibition of epidermal growth factor receptor (EGFR) with MM151 in EGFR-dependent and in cetuximab-resistant human colorectal cancer cells

doi: 10.18632/oncotarget.19797

Figure Lengend Snippet: (A-C) SW48, LIM1215 or CACO2 human colon cancer cells were injected subcutaneously into the right flank of seven nude mice, respectively. After two weeks mice were treated with cetuximab (25 mg/Kg once a week) by i.p. injection. Treatment was continued until disease progression. The black arrows indicate the time of progression to cetuximab. At progression mice were treated with MM151 (25 mg/Kg once a week) by i.p. injection. The treatment was continued until 30 weeks following tumor cell injection. At week 30, five out of seven mice were still on treatment with MM151 in the SW48 and LIM1215 xenograft groups as well as four out of seven in the CACO2 xenograft group (as indicated by double asterisk). Abbreviations: PD, progression disease; PR, partial response; SD, stable disease; wks, weeks.

Article Snippet: The human SW48 (catalogue number: HTL99020) ( KRAS, NRAS, BRAF and PIK3CA wild type) colon cancer cell line was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Injection, Biomarker Discovery

(A-C) Tumors were collected at the beginning of cetuximab treatment and at the onset of resistance to cetuximab from mice engrafted with the SW48, LIM1215 and CACO2 cell lines. As control we used one mouse that has not undergone to any type of treatment from the first in vivo experiment. Tumour samples were collected and total cell protein extracts were subjected to immunoblotting with the indicated antibodies, as described in Materials and Methods. Anti-tubulin antibody was used for normalization of protein extract content.

Journal: Oncotarget

Article Title: Antitumor efficacy of triple monoclonal antibody inhibition of epidermal growth factor receptor (EGFR) with MM151 in EGFR-dependent and in cetuximab-resistant human colorectal cancer cells

doi: 10.18632/oncotarget.19797

Figure Lengend Snippet: (A-C) Tumors were collected at the beginning of cetuximab treatment and at the onset of resistance to cetuximab from mice engrafted with the SW48, LIM1215 and CACO2 cell lines. As control we used one mouse that has not undergone to any type of treatment from the first in vivo experiment. Tumour samples were collected and total cell protein extracts were subjected to immunoblotting with the indicated antibodies, as described in Materials and Methods. Anti-tubulin antibody was used for normalization of protein extract content.

Article Snippet: The human SW48 (catalogue number: HTL99020) ( KRAS, NRAS, BRAF and PIK3CA wild type) colon cancer cell line was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Control, In Vivo, Western Blot

The SW48, SW48-CR, HCT15 and SW480 cancer cells were treated with silybin (90 μM) or regorafenib (2 μM) and their combination for 72 hours. After 14 days the colonies were stained with 0.1% crystal violet and counted as described in Materials and Methods. ( A ) Images of colon cancer cells acquired by phase-contrast microscope. ( B ) Histogram of colony number counted by image j plugin. Error bars indicate the standard deviation. * p < 0.05 compared to single treatment. The effects of treatments were also evaluated in terms of oxidative stress generation as described in Materials and Methods. ( C ) Histogram of DHE mean fluorescence intensity (% of control). Error bars indicate the standard deviation. * p < 0.05 compared to positive control. ( D ) Flow cytometry overlay of dihydroethidium (DHE) fluorescence intensity within HCT15 cells.

Journal: Oncotarget

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer

doi: 10.18632/oncotarget.20054

Figure Lengend Snippet: The SW48, SW48-CR, HCT15 and SW480 cancer cells were treated with silybin (90 μM) or regorafenib (2 μM) and their combination for 72 hours. After 14 days the colonies were stained with 0.1% crystal violet and counted as described in Materials and Methods. ( A ) Images of colon cancer cells acquired by phase-contrast microscope. ( B ) Histogram of colony number counted by image j plugin. Error bars indicate the standard deviation. * p < 0.05 compared to single treatment. The effects of treatments were also evaluated in terms of oxidative stress generation as described in Materials and Methods. ( C ) Histogram of DHE mean fluorescence intensity (% of control). Error bars indicate the standard deviation. * p < 0.05 compared to positive control. ( D ) Flow cytometry overlay of dihydroethidium (DHE) fluorescence intensity within HCT15 cells.

Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Staining, Microscopy, Standard Deviation, Fluorescence, Control, Positive Control, Flow Cytometry

( A ) Apoptosis was evaluated with Annexin-V-FITC staining and 7-Amino-Actinomycin D (7-AAD) detection assays using flow cytometry in SW48, SW48-CR, HCT15 and SW480 cancer cells after 24 hours of incubation with silybin (90 μM) or regorafenib (2 μM) and their combination. Histogram of data expressed as percentage of apoptotic cells.* p < 0.05 compared to single treatment. ( B ) Colon cancer cells were treated with silybin (90 μM) or regorafenib (2 μM) and their combination for 24 hours. Expression of PARP, caspase 3 and 9 were evaluated by immunoblotting as described in Materials and Methods. α-Tubulin was used as the loading control.

Journal: Oncotarget

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer

doi: 10.18632/oncotarget.20054

Figure Lengend Snippet: ( A ) Apoptosis was evaluated with Annexin-V-FITC staining and 7-Amino-Actinomycin D (7-AAD) detection assays using flow cytometry in SW48, SW48-CR, HCT15 and SW480 cancer cells after 24 hours of incubation with silybin (90 μM) or regorafenib (2 μM) and their combination. Histogram of data expressed as percentage of apoptotic cells.* p < 0.05 compared to single treatment. ( B ) Colon cancer cells were treated with silybin (90 μM) or regorafenib (2 μM) and their combination for 24 hours. Expression of PARP, caspase 3 and 9 were evaluated by immunoblotting as described in Materials and Methods. α-Tubulin was used as the loading control.

Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Staining, Flow Cytometry, Incubation, Expressing, Western Blot, Control

SW48, SW48-CR, HCT15 and SW480 cancer cells were treated with silybin or regorafenib and their combination at the indicated doses for 24 hours. Total cell protein extracts were subjected to immunoblotting with the indicated antibodies as described in Materials and Methods. α-Tubulin was used as the loading control.

Journal: Oncotarget

Article Title: Regorafenib in combination with silybin as a novel potential strategy for the treatment of metastatic colorectal cancer

doi: 10.18632/oncotarget.20054

Figure Lengend Snippet: SW48, SW48-CR, HCT15 and SW480 cancer cells were treated with silybin or regorafenib and their combination at the indicated doses for 24 hours. Total cell protein extracts were subjected to immunoblotting with the indicated antibodies as described in Materials and Methods. α-Tubulin was used as the loading control.

Article Snippet: The human SW48 colon cancer cell ( KRAS, NRAS, BRAF and PIK3CA wild-type profile) was obtained from IRCCS “Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genova” Italy.

Techniques: Western Blot, Control