mda231 Search Results


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clea japan inc mda-231 cells
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Genentech inc mda-231
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BioResource International Inc mda 231-brm2-831 (gfp+/luciferase+) cells
Mda 231 Brm2 831 (Gfp+/Luciferase+) Cells, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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INOVOTION mb−mda−231 cell line
Mb−Mda−231 Cell Line, supplied by INOVOTION, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pasteur Institute cancer cell lines mda 231
Effect of IC 50 Concentration of TCE on <t>A549,</t> MCF-7, and MDA-231 Cell Proliferation: TCE decreased the cell survival to 17.6%, 21.4%, and 27.21 in 200 µg concentration compared to the control cells
Cancer Cell Lines Mda 231, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Korean Cell Line Bank mda-231
Effect of IC 50 Concentration of TCE on <t>A549,</t> MCF-7, and MDA-231 Cell Proliferation: TCE decreased the cell survival to 17.6%, 21.4%, and 27.21 in 200 µg concentration compared to the control cells
Mda 231, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory gfp+/luc + mda-231 cells
Effect of IC 50 Concentration of TCE on <t>A549,</t> MCF-7, and MDA-231 Cell Proliferation: TCE decreased the cell survival to 17.6%, 21.4%, and 27.21 in 200 µg concentration compared to the control cells
Gfp+/Luc + Mda 231 Cells, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Charles River Laboratories 10 6 mda-231 cells
Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of <t>MDA-231</t> (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)
10 6 Mda 231 Cells, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Stemline Therapeutics mda-231 cell line
Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of <t>MDA-231</t> (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)
Mda 231 Cell Line, supplied by Stemline Therapeutics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Keio University Press Inc mda231
Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of <t>MDA-231</t> (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)
Mda231, supplied by Keio University Press Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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European Collection of Authenticated Cell Cultures breast carcinoma mda231- tgl cells
Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of <t>MDA-231</t> (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)
Breast Carcinoma Mda231 Tgl Cells, supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Effect of IC 50 Concentration of TCE on A549, MCF-7, and MDA-231 Cell Proliferation: TCE decreased the cell survival to 17.6%, 21.4%, and 27.21 in 200 µg concentration compared to the control cells

Journal: Asian Pacific Journal of Cancer Prevention : APJCP

Article Title: Terminalia Catappa Extract (TCE) Reduces Proliferation of Lung and Breast Cancer Cell by Modulating miR-21 and miR-34a Expressions

doi: 10.31557/APJCP.2021.22.4.1157

Figure Lengend Snippet: Effect of IC 50 Concentration of TCE on A549, MCF-7, and MDA-231 Cell Proliferation: TCE decreased the cell survival to 17.6%, 21.4%, and 27.21 in 200 µg concentration compared to the control cells

Article Snippet: Cancer Cell Cultures MCF7, MDA 231, and A549 cancer cell lines were obtained from the Pasteur Institute of Iran (Tehran, Iran).

Techniques: Concentration Assay, Control

Effects of TCE Treatment on the Expression of BAX, Bcl-2, MMP-13, miR-21, miR-34a, Cas-3, Cas-8, Cas-9 and Vimentin in A549 Cell Line. The data was presented as mean ± SD (N=3) (* = P< 0.05).

Journal: Asian Pacific Journal of Cancer Prevention : APJCP

Article Title: Terminalia Catappa Extract (TCE) Reduces Proliferation of Lung and Breast Cancer Cell by Modulating miR-21 and miR-34a Expressions

doi: 10.31557/APJCP.2021.22.4.1157

Figure Lengend Snippet: Effects of TCE Treatment on the Expression of BAX, Bcl-2, MMP-13, miR-21, miR-34a, Cas-3, Cas-8, Cas-9 and Vimentin in A549 Cell Line. The data was presented as mean ± SD (N=3) (* = P< 0.05).

Article Snippet: Cancer Cell Cultures MCF7, MDA 231, and A549 cancer cell lines were obtained from the Pasteur Institute of Iran (Tehran, Iran).

Techniques: Expressing

Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of MDA-231 (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)

Journal: Cancer Drug Resistance

Article Title: EGFR signaling promotes resistance to CHK1 inhibitor prexasertib in triple negative breast cancer

doi: 10.20517/cdr.2020.73

Figure Lengend Snippet: Erlotinib co-exposure with prexasertib synergistically enhanced cell killing. Viability of 3D cultures of MDA-231 (A) and MDA-468 (B) after exposure to prexasertib, erlotinib, and combinations of erlotinib and prexasertib; the combination index (CI) showed synergistic interaction (CI < 1) of erlotinib and prexasertib in both MDA-231 and MDA-468 (C)

Article Snippet: Forty athymic nude mice (Charles River) were implanted subcutaneously with 10 6 MDA-231 cells or 10 7 MDA-468 cells 1:1 in low growth factor Matrigel.

Techniques:

Erlotinib co-exposure with prexasertib reduced BAD phosphorylation. MDA-231 cells treated with vehicle, 20 nmol/L prexasertib, 10 µmol/L erlotinib, or both 20 nmol/L prexasertib and 10 µmol/L erlotinib at 48 and 72 h (A); MDA-468 cells treated with vehicle, 20 nmol/L prexasertib, 10 µmol/L erlotinib, or both 20 nmol/L prexasertib and 10 µmol/L erlotinib at 48 and 72 h (B)

Journal: Cancer Drug Resistance

Article Title: EGFR signaling promotes resistance to CHK1 inhibitor prexasertib in triple negative breast cancer

doi: 10.20517/cdr.2020.73

Figure Lengend Snippet: Erlotinib co-exposure with prexasertib reduced BAD phosphorylation. MDA-231 cells treated with vehicle, 20 nmol/L prexasertib, 10 µmol/L erlotinib, or both 20 nmol/L prexasertib and 10 µmol/L erlotinib at 48 and 72 h (A); MDA-468 cells treated with vehicle, 20 nmol/L prexasertib, 10 µmol/L erlotinib, or both 20 nmol/L prexasertib and 10 µmol/L erlotinib at 48 and 72 h (B)

Article Snippet: Forty athymic nude mice (Charles River) were implanted subcutaneously with 10 6 MDA-231 cells or 10 7 MDA-468 cells 1:1 in low growth factor Matrigel.

Techniques:

EGF stimulation in MDA-231 increased BAD phosphorylation. MDA-231 cells treated with vehicle, 20 nmol/L prexasertib, 50 nmol/L EGF, or both 50 nmol/L EGF and 20 nmol/L prexasertib were examined after 48 h of exposure. AKT: protein kinase B; EGF: epidermal growth factor; EGFR: epidermal growth factor receptor

Journal: Cancer Drug Resistance

Article Title: EGFR signaling promotes resistance to CHK1 inhibitor prexasertib in triple negative breast cancer

doi: 10.20517/cdr.2020.73

Figure Lengend Snippet: EGF stimulation in MDA-231 increased BAD phosphorylation. MDA-231 cells treated with vehicle, 20 nmol/L prexasertib, 50 nmol/L EGF, or both 50 nmol/L EGF and 20 nmol/L prexasertib were examined after 48 h of exposure. AKT: protein kinase B; EGF: epidermal growth factor; EGFR: epidermal growth factor receptor

Article Snippet: Forty athymic nude mice (Charles River) were implanted subcutaneously with 10 6 MDA-231 cells or 10 7 MDA-468 cells 1:1 in low growth factor Matrigel.

Techniques:

Co-exposure of erlotinib and prexasertib significantly reduced tumor progression in MDA-231 and MDA-468 xenografts. MDA-231 and MDA-468 xenograft containing mice were treated with vehicle, 10 mg/kg BW prexasertib, 50 mg/kg BW erlotinib, or both prexasertib and erlotinib (A); tumor weights at sacrifice for MDA-231 and MDA-468 (B)

Journal: Cancer Drug Resistance

Article Title: EGFR signaling promotes resistance to CHK1 inhibitor prexasertib in triple negative breast cancer

doi: 10.20517/cdr.2020.73

Figure Lengend Snippet: Co-exposure of erlotinib and prexasertib significantly reduced tumor progression in MDA-231 and MDA-468 xenografts. MDA-231 and MDA-468 xenograft containing mice were treated with vehicle, 10 mg/kg BW prexasertib, 50 mg/kg BW erlotinib, or both prexasertib and erlotinib (A); tumor weights at sacrifice for MDA-231 and MDA-468 (B)

Article Snippet: Forty athymic nude mice (Charles River) were implanted subcutaneously with 10 6 MDA-231 cells or 10 7 MDA-468 cells 1:1 in low growth factor Matrigel.

Techniques: