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Structured Review

Asterand Inc human ibc cell line sum149
Human Ibc Cell Line Sum149, supplied by Asterand Inc, 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+ibc+cell+line+sum149/sum149+cells/pm40329335-66-1-9
Average 90 stars, based on 1 article reviews
human ibc cell line sum149 - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Suspension:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Staining:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Immunohistochemistry:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Expressing:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

In Vivo:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Migration:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

In Vitro:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Western Blot:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Transwell Migration Assay:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Tube Formation Assay:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Comparison:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Cell Culture:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

CtB Assay:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Control:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Knockdown:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Flow Cytometry:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Quantitative RT-PCR:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Over Expression:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Derivative Assay:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Enzyme-linked Immunosorbent Assay:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Recombinant:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Two Tailed Test:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Fluorescence:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Transfection:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Injection:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).

Ex Vivo:

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization.
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda MericBernstam (The University of Texas MD Anderson Cancer Center).

Article Title: AXL promotes inflammatory breast cancer progression by regulating immunosuppressive macrophage polarization
Article Snippet: The human IBC cell line SUM149 was purchased from Asterand (Detroit, MI), and the human IBC cell line BCX010 was provided by Dr. Funda Meric-Bernstam (The University of Texas MD Anderson Cancer Center).



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Asterand Inc human ibc cell line sum149
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In vitro VEGF (0.62, 1.25, 2.5 uM), SU5416, bevacizumab and celecoxib (1.5, 3, 6 uM) effects on cell viability after 24 h, 48 h and 72 h post-treatment in IPC-366 and <t>SUM149</t> cell lines measured by MTS assay. Cell viability increases after VEGF addition in both cell lines ( A , B ). Cell viability decreased after SU5416 treatment in IPC-366 cells and increased in SUM149-treated cells ( C , D ). Decreased cell viability in IPC-366- and SUM149 treated cells after bevacizumab ( E , F ) and celecoxib ( G , H ) addition. Data are shown as means ± SEM. * Significant differences between control and treated groups ( p < 0.05).
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Image Search Results


In vitro VEGF (0.62, 1.25, 2.5 uM), SU5416, bevacizumab and celecoxib (1.5, 3, 6 uM) effects on cell viability after 24 h, 48 h and 72 h post-treatment in IPC-366 and SUM149 cell lines measured by MTS assay. Cell viability increases after VEGF addition in both cell lines ( A , B ). Cell viability decreased after SU5416 treatment in IPC-366 cells and increased in SUM149-treated cells ( C , D ). Decreased cell viability in IPC-366- and SUM149 treated cells after bevacizumab ( E , F ) and celecoxib ( G , H ) addition. Data are shown as means ± SEM. * Significant differences between control and treated groups ( p < 0.05).

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: In vitro VEGF (0.62, 1.25, 2.5 uM), SU5416, bevacizumab and celecoxib (1.5, 3, 6 uM) effects on cell viability after 24 h, 48 h and 72 h post-treatment in IPC-366 and SUM149 cell lines measured by MTS assay. Cell viability increases after VEGF addition in both cell lines ( A , B ). Cell viability decreased after SU5416 treatment in IPC-366 cells and increased in SUM149-treated cells ( C , D ). Decreased cell viability in IPC-366- and SUM149 treated cells after bevacizumab ( E , F ) and celecoxib ( G , H ) addition. Data are shown as means ± SEM. * Significant differences between control and treated groups ( p < 0.05).

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: In Vitro, MTS Assay, Control

Tube formation results. ( A ) Images ×10 of IPC-366 and SUM149 vascular-like structures (arrows) formed in control and treated groups treated with a final concentration of 1.5 uM for VEGF, SU5416, bevacizumab and celecoxib. Bar graph represents percentage of number of tubes formed at 6 h respect to control group. ( B ) Steroid precursor (P4, DHEA, A4); ( C ) sexual steroids (T, DHT, E2, E1SO4) and ( D ) angiogenic growth factors (VEGF-A, VEGF-C, VEGF-D, IL-8) in culture media of IPC-366 (black) and SUM149 (grey) after tube formation assay. * Denoted significant differences ( p < 0.05) between control and treated groups. Scale bar 200 µM.

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: Tube formation results. ( A ) Images ×10 of IPC-366 and SUM149 vascular-like structures (arrows) formed in control and treated groups treated with a final concentration of 1.5 uM for VEGF, SU5416, bevacizumab and celecoxib. Bar graph represents percentage of number of tubes formed at 6 h respect to control group. ( B ) Steroid precursor (P4, DHEA, A4); ( C ) sexual steroids (T, DHT, E2, E1SO4) and ( D ) angiogenic growth factors (VEGF-A, VEGF-C, VEGF-D, IL-8) in culture media of IPC-366 (black) and SUM149 (grey) after tube formation assay. * Denoted significant differences ( p < 0.05) between control and treated groups. Scale bar 200 µM.

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: Control, Concentration Assay, Tube Formation Assay

In vivo effect of VEGF, SU5416, bevacizumab and celecoxib on tumour growth in xenotransplanted mice of ( A , C , E , G ) IPC-366 and ( B , D , F , H ) SUM149. Bar represents means ± SEM. * Significant differences between control and treatment groups ( p < 0.05).

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: In vivo effect of VEGF, SU5416, bevacizumab and celecoxib on tumour growth in xenotransplanted mice of ( A , C , E , G ) IPC-366 and ( B , D , F , H ) SUM149. Bar represents means ± SEM. * Significant differences between control and treatment groups ( p < 0.05).

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: In Vivo, Control

Foci of pulmonary and hepatic metastasis in control and experimental groups of IPC-366 and  SUM149.

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: Foci of pulmonary and hepatic metastasis in control and experimental groups of IPC-366 and SUM149.

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: Control

Metastatic foci in lungs and liver after VEGF, SU5416, bevacizumab and celecoxib treatment in IPC-366 and SUM149 xenotransplanted mice. ( A ) SUM149 control mice lung with metastatic focus. ( B ) IPC-336 control mice liver with large metastic focus. ( C , D ). Foci of metastases in lung and liver after VEGF inoculation in IPC-366- (c) and SUM149- (d) xenotransplanted mice. ( F ) Multiple small foci of metastasis in the lung of SUM-149 mice treated with 5 mg/kg of SU5416. ( G , H ). Absence of metastatic foci after bevacizumab treatment in IPC-366 xenografted mice. ( I ) Small foci of metastasis after inoculation (0.5 mg/kg) of celecoxib.

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: Metastatic foci in lungs and liver after VEGF, SU5416, bevacizumab and celecoxib treatment in IPC-366 and SUM149 xenotransplanted mice. ( A ) SUM149 control mice lung with metastatic focus. ( B ) IPC-336 control mice liver with large metastic focus. ( C , D ). Foci of metastases in lung and liver after VEGF inoculation in IPC-366- (c) and SUM149- (d) xenotransplanted mice. ( F ) Multiple small foci of metastasis in the lung of SUM-149 mice treated with 5 mg/kg of SU5416. ( G , H ). Absence of metastatic foci after bevacizumab treatment in IPC-366 xenografted mice. ( I ) Small foci of metastasis after inoculation (0.5 mg/kg) of celecoxib.

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: Control

In vivo tumour homogenate and serum sex steroid hormones, angiogenic growth factors and IL-8 concentrations in IPC-366- and SUM149 xenotransplanted mice after inoculation of the high dosage of VEGF (1 mg/kg), SU5416 (10 mg/kg), bevacizumab (10 mg/kg) and celecoxib treatment (5 mg/kg). Bar represents means ± SEM. * Significant differences between control and treatment groups ( p < 0.05). ( A ) Serum P4 levels were no altered but its intratumoral concentrations decreased after SU5416 and celecoxib. ( B ) Serum DHEA levels decreased after VEGF, SU5416 and celecoxib and no changes in its intratumoral concentrations were found after all treatments. ( C ) Serum and intratumoral A4 levels decreased after VEGF, bevacizumab and celecoxib. ( D ) Serum T levels decreased after SU5416 and celecoxib, but tumour homogenate levels were higher after all treatments. ( E ) Both serum and intratumoral DHT levels decreased after SU5416 and bevacizumab. ( F ) VEGF and SU5416 inoculation diminished circulating E1SO4 levels but augmented its intratumoral concentrations. ( G ) Serum E2 levels decreased after VEGF but augmented after SU5416, however, tumour homogenate concentrations were higher after VEGF but decreased after bevacizumab and celecoxib ( H ) Circulating and intratumoral VEGF-A levels augmented after VEGF inoculation, but these concentrations decreased only after bevacizumab. ( I ) VEGF and SU5416 treatments decreased circulating VEGF-C levels and celecoxib augmented them, however, only VEGF and SU5416 decreased intratumoral concentrations. ( J ) Only serum VEGF-D levels were augmented after VEGF and SU5416 treatments. ( K ) Serum IL-8 levels decreased after the inoculation of SU5416, bevacizumab and celecoxib, whereas its tumour levels decreased after VEGF and SU5416 but augmented after celecoxib.

Journal: Cancers

Article Title: Anti-Angiogenic Treatments Interact with Steroid Secretion in Inflammatory Breast Cancer Triple Negative Cell Lines

doi: 10.3390/cancers13153668

Figure Lengend Snippet: In vivo tumour homogenate and serum sex steroid hormones, angiogenic growth factors and IL-8 concentrations in IPC-366- and SUM149 xenotransplanted mice after inoculation of the high dosage of VEGF (1 mg/kg), SU5416 (10 mg/kg), bevacizumab (10 mg/kg) and celecoxib treatment (5 mg/kg). Bar represents means ± SEM. * Significant differences between control and treatment groups ( p < 0.05). ( A ) Serum P4 levels were no altered but its intratumoral concentrations decreased after SU5416 and celecoxib. ( B ) Serum DHEA levels decreased after VEGF, SU5416 and celecoxib and no changes in its intratumoral concentrations were found after all treatments. ( C ) Serum and intratumoral A4 levels decreased after VEGF, bevacizumab and celecoxib. ( D ) Serum T levels decreased after SU5416 and celecoxib, but tumour homogenate levels were higher after all treatments. ( E ) Both serum and intratumoral DHT levels decreased after SU5416 and bevacizumab. ( F ) VEGF and SU5416 inoculation diminished circulating E1SO4 levels but augmented its intratumoral concentrations. ( G ) Serum E2 levels decreased after VEGF but augmented after SU5416, however, tumour homogenate concentrations were higher after VEGF but decreased after bevacizumab and celecoxib ( H ) Circulating and intratumoral VEGF-A levels augmented after VEGF inoculation, but these concentrations decreased only after bevacizumab. ( I ) VEGF and SU5416 treatments decreased circulating VEGF-C levels and celecoxib augmented them, however, only VEGF and SU5416 decreased intratumoral concentrations. ( J ) Only serum VEGF-D levels were augmented after VEGF and SU5416 treatments. ( K ) Serum IL-8 levels decreased after the inoculation of SU5416, bevacizumab and celecoxib, whereas its tumour levels decreased after VEGF and SU5416 but augmented after celecoxib.

Article Snippet: The SUM149 triple-negative human IBC cell line was originally obtained from Asterand, Plc. (Detroit, MI, USA) and was grown in Ham’s F-12 medium (Invitrogen, 21765029) supplemented with 5% FBS (Sigma Aldrich, 12103C), 1 ug/mL hydrocortisone (Sigma Aldrich, H4001), 5 ug/mL insulin (Sigma Aldrich, I9278) and 1% penicillin-streptomycin solution (Sigma Aldrich, P0781).

Techniques: In Vivo, Control