lncap cell Search Results


94
CLS Cell Lines Service GmbH lncap
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Lncap, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lncap/product/CLS Cell Lines Service GmbH
Average 94 stars, based on 1 article reviews
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93
Santa Cruz Biotechnology lncap cell lysates
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Lncap Cell Lysates, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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90
Korean Cell Line Bank lncap cells
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Lncap Cells, 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
https://www.bioz.com/result/lncap cells/product/Korean Cell Line Bank
Average 90 stars, based on 1 article reviews
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90
China Center for Type Culture Collection lncap cell line
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Lncap Cell Line, supplied by China Center for Type Culture Collection, 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/result/lncap cell line/product/China Center for Type Culture Collection
Average 90 stars, based on 1 article reviews
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90
Shanghai Genechem Ltd cell line lncap
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Cell Line Lncap, supplied by Shanghai Genechem Ltd, 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/result/cell line lncap/product/Shanghai Genechem Ltd
Average 90 stars, based on 1 article reviews
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90
Eurobio hormone-sensitive lncap cell line
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Hormone Sensitive Lncap Cell Line, supplied by Eurobio, 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/result/hormone-sensitive lncap cell line/product/Eurobio
Average 90 stars, based on 1 article reviews
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90
Dainippon Sumitomo human prostate cancer cell lines lncap and pc-3
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Human Prostate Cancer Cell Lines Lncap And Pc 3, supplied by Dainippon Sumitomo, 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/result/human prostate cancer cell lines lncap and pc-3/product/Dainippon Sumitomo
Average 90 stars, based on 1 article reviews
human prostate cancer cell lines lncap and pc-3 - by Bioz Stars, 2026-04
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90
Gemini Bio prostate cancer cell lines lncap, c4-2, or c4-2b4
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Prostate Cancer Cell Lines Lncap, C4 2, Or C4 2b4, supplied by Gemini Bio, 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/result/prostate cancer cell lines lncap, c4-2, or c4-2b4/product/Gemini Bio
Average 90 stars, based on 1 article reviews
prostate cancer cell lines lncap, c4-2, or c4-2b4 - by Bioz Stars, 2026-04
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90
Korean Cell Line Bank lncap androgen receptor dependent cell line
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Lncap Androgen Receptor Dependent Cell Line, 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
https://www.bioz.com/result/lncap androgen receptor dependent cell line/product/Korean Cell Line Bank
Average 90 stars, based on 1 article reviews
lncap androgen receptor dependent cell line - by Bioz Stars, 2026-04
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90
Pasteur Institute human prostate carcinoma cell line lncap
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Human Prostate Carcinoma Cell Line Lncap, 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
https://www.bioz.com/result/human prostate carcinoma cell line lncap/product/Pasteur Institute
Average 90 stars, based on 1 article reviews
human prostate carcinoma cell line lncap - by Bioz Stars, 2026-04
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90
National Centre for Cell Science human lung fibroblast cells mrc-5
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Human Lung Fibroblast Cells Mrc 5, supplied by National Centre for Cell Science, 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/result/human lung fibroblast cells mrc-5/product/National Centre for Cell Science
Average 90 stars, based on 1 article reviews
human lung fibroblast cells mrc-5 - by Bioz Stars, 2026-04
90/100 stars
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90
Sangon Biotech human prostate lncap cancer cell line
Inhibition of the proliferation of <t>human</t> <t>prostate</t> cancer cell lines <t>LNCaP</t> and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).
Human Prostate Lncap Cancer Cell Line, supplied by Sangon Biotech, 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/result/human prostate lncap cancer cell line/product/Sangon Biotech
Average 90 stars, based on 1 article reviews
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Image Search Results


NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Cell Culture, Control, Membrane

NIPP inhibits the proliferation of tumor cells. ( A ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were categorized based on their distance from NIPP to the medium surface: the control group, 1 cm group, 3 cm group, and 6 cm group. All groups, except the control group, were exposed to NIPP for 4 min. Each experiment was conducted at least three times. ( B ): Visualization of NIPP treatment tumor cells with different distances. ( C ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were organized based on the treatment time of NIPP for the tumor cells: the control group, 1 min group, 2 min group, and 4 min group. Except for the control group, the distance of NIPP from the culture medium was 1 cm for all groups. ( D ): Visualization of NIPP treatment tumor cells with different duration. Each experiment was repeated at least three times. ( E ): Wound-healing Test of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells at 0 and 24 h. Each experimental group was compared with the control group.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP inhibits the proliferation of tumor cells. ( A ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were categorized based on their distance from NIPP to the medium surface: the control group, 1 cm group, 3 cm group, and 6 cm group. All groups, except the control group, were exposed to NIPP for 4 min. Each experiment was conducted at least three times. ( B ): Visualization of NIPP treatment tumor cells with different distances. ( C ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were organized based on the treatment time of NIPP for the tumor cells: the control group, 1 min group, 2 min group, and 4 min group. Except for the control group, the distance of NIPP from the culture medium was 1 cm for all groups. ( D ): Visualization of NIPP treatment tumor cells with different duration. Each experiment was repeated at least three times. ( E ): Wound-healing Test of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells at 0 and 24 h. Each experimental group was compared with the control group.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Control

NIPP treatment alters the cytoskeletal organization of tumor cells and glucose consumption in tumor cell culture medium. ( A ): Immunofluorescence of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. Green represents F-actin, and Blue represents the Nucleus. Magnification 20×. Next row of pictures are partial screenshots from the previous row. ( B ): Glucose relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( C ): Lactate relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP treatment alters the cytoskeletal organization of tumor cells and glucose consumption in tumor cell culture medium. ( A ): Immunofluorescence of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. Green represents F-actin, and Blue represents the Nucleus. Magnification 20×. Next row of pictures are partial screenshots from the previous row. ( B ): Glucose relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( C ): Lactate relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Cell Culture, Immunofluorescence, Control

NIPP increases LDH release in tumor cell cultures and induced no significante alterations of SOD levels in tumor cell. ( A ): LDH relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 30 min and 24 h. ( B ): SOD relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP increases LDH release in tumor cell cultures and induced no significante alterations of SOD levels in tumor cell. ( A ): LDH relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 30 min and 24 h. ( B ): SOD relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Control

( A ): Quantification of HSP27 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP27 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP40 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP40 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP70 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP70 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP90α relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP90α relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP90β relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP90β relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

Inhibition of the proliferation of human prostate cancer cell lines LNCaP and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).

Journal: British Journal of Cancer

Article Title: Insulin-like growth factor binding protein-6 inhibits prostate cancer cell proliferation: implication for anticancer effect of diethylstilbestrol in hormone refractory prostate cancer

doi: 10.1038/sj.bjc.6602520

Figure Lengend Snippet: Inhibition of the proliferation of human prostate cancer cell lines LNCaP and PC-3 by diethylstilbestrol (DES). Cells were incubated for 24 h, and thereafter CM was aspirated away and the cells were incubated with CM containing various concentrations of DES. After 72 h, the number of viable cells was measured by MTT assay. Optical densities (OD) of cell lysates were measured at a wavelength of 540 nm. The values are expressed as means+s.d. ( n =3), and the P -values were <0.05 ( * ) and <0.01 (†).

Article Snippet: The human prostate cancer cell lines LNCaP and PC-3 were purchased from Dainippon Pharmaceutical (Tokyo, Japan) and cultured in RPMI (Sigma, St Louis, MO, USA) supplemented with 10% fetal calf serum (FCS) (Moregate, Bulimba, Australia).

Techniques: Inhibition, Incubation, MTT Assay