Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: Pannexin 1 is expressed in patient-derived primary melanoma tumors, as well nodal and distant melanoma metastases. ( A ) Gene expression analyses from microarray study GSE15605 revealed significantly higher PANX1 expression in primary human melanoma tumors relative to normal skin biopsies. ( B ) Analysis of PANX1 mRNA expression in melanoma tumors of the Cancer Genome Atlas (TCGA) database revealed that PANX1 expression is not significantly different across melanoma stages (denoted according to the Cancer Tumor Stage Code). ( C ) Representative PANX1 protein levels in patient-derived melanoma tumors. Numbers represent different patient donors. A peptide pre-absorption assay confirms antibody specificity. Protein sizes in kDa. ( D ) Densitometry was used to quantify PANX1 levels (bands in bracket) in all primary, nodal and distant melanoma samples provided by the Ontario Institute for Cancer Research (OICR), normalized to GADPH (Sample 9 was degraded and not used for analysis). There is no significant difference in PANX1 levels among stages of melanoma progression. Primary tumors (N = 6 patients, n = 27 technical reps), Nodal mets (N = 7, n = 29), Distant mets (N = 3, n = 13); One-way ANOVA followed by Tukey’s post-hoc test was used to analyze data. line = mean; NS = not significant. ( E ) Patient-derived primary melanoma tumor labeled with PANX1 (green). Sequential sections of the tumor stained using H&E (provided by OICR) and a marker for a melanocytic-lineage, MITF (red). Melanoma core (C), Necrotic regions of the tumor (N), Stromal area of the tumor (S). Bar: 1000 μm.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Derivative Assay, Expressing, Microarray, Labeling, Staining, Marker

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: PANX1 is highly expressed in patient-derived primary melanoma cells. ( A ) Representative PANX1 levels in primary cells derived from melanoma biopsies of patient tumors with primary (N = 5), nodal (N = 4) and distant (N = 4) metastases. Cultures of primary melanoma cells were distinguished through MITF expression. ( B ) Patient-derived primary melanoma cells extracted from three stages of melanoma progression express PANX1 intracellularly and at the cell membrane. MITF is a transcription factor involved in melanocytic lineages and is found in the nucleus and in the cytoplasm of the cell. ( C ) Patient-matched primary cells were extracted from a primary tumor and a nodal metastasis within a single patient and show high PANX1 levels. Melanoma identity was confirmed with MITF expression. ( D ) Patient-matched primary cells immunolabeled for PANX1 show intracellular and cell membrane localization. PANX1: green, MITF: red, Hoechst: blue; Bar: 20 μm.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Derivative Assay, Expressing, Immunolabeling

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: Pannexin 1 is expressed in established human melanoma cell lines. ( A ) A375-P and A375-MA2 human melanoma cells were fixed and stained with anti-PANX1 polyclonal antibodies (green). DNA was stained with Hoechst (blue). Bar: 20 μm. Representative fields are shown from three separate experiments. ( B ) A375-P, A375-MA2, Normal Rat Kidney cells (NRK), and NRK overexpressing PANX1 (NRK-PANX1) cells were lysed and equal amounts of protein were resolved by SDS-PAGE. The blots were probed with the anti-PANX1 antibodies. Black line denotes that both images are from the same blot but scanned with different intensity. Right panel shows the quantification of PANX1 bands in A375-P and A375-MA2 samples using ImageStudio 3.0. The data are expressed as means ±SEM (N = 4) Statistical analyses using student’s t -tests; * p < 0.05. ( C ) A375-P and A375-MA2 melanoma cells were cultured at 20,000 cells per well in medium containing 10% FBS. Cells were counted daily up to 4 days after initial seeding of the cells onto the 24-well culture dish. The data are expressed as mean ± SEM (N = 5, n = 25). Two-way ANOVA was used to statistically analyze data. * p < 0.05, ** p < 0.01. ( D ) Scratch assays were performed on a confluent monolayer of A375-P and A375-MA2 cells to assess migration. Quantifications represents cell migration three days following the initial scratch and treatment application. Statistical analysis was performed using student’s t -tests; *** p < 0.001. ( E ) Melanin was extracted from one million A375-P and A375-MA2 cells. There was significantly decreased melanin content detected in A375-MA2 compared to A375-P cells at the same passage number. Statistical analyses for melanin extraction data includes student’s t -tests; * p < 0.05.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Staining, SDS Page, Cell Culture, Migration

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: Knocking down PANX1 reduces growth and migration in human melanoma cells. ( A ) A375-P and A375-MA2 cells were transfected with either scrambled shRNA (SCRsh) as a control or shRNA constructs against PANX1 (PANX1sh). Western blot analysis confirmed PANX1 knockdown in both cell lines. GAPDH was used as loading control. Dotted line indicates extra lanes removed from the same blot scanned at the same intensity. Graphs depict the quantification of Western blots from three separate experiments conducted on different cell lysates, N = 3, student’s t -tests; **** p < 0.0001, ** p < 0.001 ( B ) PANX1 mRNA levels were measured by qPCR in control and PANX1 knockdown A375-P cells. Values in control samples were set to 1. Data are expressed as mean ± SEM, (N = 3, n = 9). Student’s t -test was used to analyse data; **** p < 0.0001. ( C ) A375-P cells transfected with scrambled shRNA (SCRshRNA, depicting PANX1 at the cell surface) or shRNA against PANX1 (PANX1shRNA, significantly reduced PANX1 signal) were fixed and stained with anti-PANX1 polyclonal antibodies (green). DNA was stained with Hoescht (blue). Staining with secondary antibody alone (2° only) was used as a control. Bar: 20 μm. ( D ) A375-P cells transfected with either scrambled shRNA (SCR shRNA) or shRNA against PANX1 (PANX1shRNA) were cultured at 20,000 cells per well in medium containing 10% FBS. Cells were counted daily up to 4 days after initial seeding of the cells onto the culture. There was a significant reduction in cell growth after three days in cells with reduced levels of PANX1. The data are expressed as mean ± SEM from four separate experiments conducted with three technical replicates. (N = 4, n = 12). Two-way ANOVA was used to statistically analyze the data. ** p < 0.01, **** p < 0.0001. E. Scratch assays were performed on a confluent monolayer of Scrambled (SCRshRNA) and PANX1 knockdown (PANX1shRNA) A375-P and A375-MA2 cells to assess migration in growth media with chFBS. The distance travelled by the cells represents cell migration three days following the initial scratch and treatment application. Data are expressed as mean ± SEM (N = 3, n = 9).

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Migration, Transfection, shRNA, Construct, Western Blot, Staining, Cell Culture

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: PANX1 blockers reduce the tumorigenic properties of human melanoma cells in vitro. A375-P melanoma cells were cultured at 20,000 cells per well in medium containing 10% FBS in the presence of PBN (1 mM) in ( A ) and CBX (100 µM) in ( B ). Similarly, A375-MA2 melanoma cells were cultured in the presence of PBN ( C ) or CBX ( D ) added to the culture medium. Cells were counted daily up to 4 days after initial seeding of the cells onto the culture. The data are expressed as mean ± SEM from three separate experiments conducted with three technical replicates. (N = 3, n = 9). ( E ) Scratch assays were performed on a confluent monolayer of A375-MA2 cells in the presence of PBN (1 mM, N = 3, n = 22) or CBX (100 µM, N = 3, n = 20) to assess migration. Data are expressed as mean ± SEM. Vehicle treated cells were used as control in the experiment. A significant decrease in A375-MA2 cell migration was noted in the presence of PBN and CBX. ( F ) Significantly more melanin was extracted from A375-MA2 cells treated with either 100 μM CBX (N = 3, n = 15) or 1 mM PBN (N = 3, n = 13) compared to vehicle controls. Statistical analyses for growth curves were performed using a two-way ANOVA followed by a Sidak test. Statistical analyses for migration assays and melanin extraction data includes student’s t -tests; * p < 0.05, *** p < 0.001, **** p < 0.0001; Bars indicate SEM.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: In Vitro, Cell Culture, Migration

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: PANX1 blockers significantly reduced A375-MA2 melanoma tumor weight and invasion in chicken embryo xenografts. ( A ) One million A375-MA2 human melanoma cells were incubated with a DiO’lipophilic cell tracer, combined with Matrigel (1:1) and seeded onto the chorioallantoic membrane (CAM) of a ten-day-old chick embryo ex vivo. A375-MA2 tumors treated for one week with 100 μM CBX (N = 16) or 1 mM PBN (N = 11). ( B ) Tumors treated with CBX or PBN weighed significantly less than tumors treated with the vehicle control (N = 15). Statistical analyses were performed using one-way ANOVA followed by a Tukey’s post-hoc test. Lines represent the mean, ** p < 0.01. ( C ) A375-MA2 melanoma tumors were extracted from the CAM on day 18 of the experiment, sectioned and stained using H&E to analyze tumor structure. Tumors treated with the vehicle control (N = 4) showed an undefined border between the tumor and the CAM, possibly due to A375-MA2 cell invasion into the CAM. In contrast, tumors treated daily with 100 μM CBX (N = 4) were more easily removed from the CAM and displayed a defined tumor edge. Arrows indicate the edge of the tumors. To quantify CAM integrity, H&E images were converted to binary and inverted. A standard frame area was used in each image to measure the mean grey intensity in pixels as a measure of the area of intact CAM-tumor interface. The area of the intact tumor border was significantly increased in A375-MA2 tumors treated daily with 100 μM CBX for one week compared to those treated with the vehicle control (N = 4, n = 12). Scale bar: 50 μm and is the same for all images in ( C ). Bars indicate mean ± SEM. ** p < 0.01.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Incubation, Ex Vivo, Staining

Journal: Cancers

Article Title: Inhibition of Pannexin 1 Reduces the Tumorigenic Properties of Human Melanoma Cells

doi: 10.3390/cancers11010102

Figure Lengend Snippet: Inhibition of PANX1 alters the signaling profile of melanoma cells. ( A ) Protein lysates from A375-P, A375-MA2 cells with endogenous expression of PANX1 as well as A375-MA2 cells overexpressing PANX1 were used for cell-surface biotinylation assays. Negative controls were prepared in parallel in absence of biotin labeling reagent. Western blotting for L1-CAM and GAPDH were used as positive control of cell surface protein and control for non-specific biotinylation of intracellular/cytoplasmic proteins, respectively. Only a fraction of PANX1 is localized to the cell surface of cells examined in this experiment. ( B ) A375-P cells were washed in PBS and incubated with appropriate isotonic solution for 5 min (100% PBS (control), 70% PBS or 30% PBS) in the presence of 1 mM PBN. There was a significant decrease in ATP released into the culture medium in the presence of 1 mM PBN. Plotted values are means ±S.D. * p < 0.05, *** p < 0.0005 as determined by a two-way ANOVA with a Tukey’s multiple comparisons test. Viable cells were counted after each treatment and plotted in the right panel. There was no significant difference in the number of live cells in each treatment condition. ( C ) A375-P cells were transfected with either scrambled shRNA (SCRshRNA) as a control or two different shRNA construct against PANX1 (PANX1shRNA -B and -D). Cells were lysed, and equal amounts of protein were resolved by 12% SDS-PAGE. Western blot analysis using polyclonal antibodies confirmed PANX1 knockdown. GAPDH was used as loading control. There was a significant reduction in the abundance of β-catenin in PANX1 knockdown cells. Cell lysates of non-transfected A375-P and A375-MA2 cells were used as additional controls in the experiments. Graph depicts the quantification of western blots from three separate experiments, N = 3, student’s t -tests; *** p < 0.0001.

Article Snippet: A375-P and A375-MA2 cells were transfected with two constructs (PANX1 shRNA-B and PANX1 shRNA-D) from Origene (Rockville, MD, USA): PANX1 human 29-mer shRNA kit in pRS vector (TR302694) plus a non-effective 29-mer scrambled shRNA cassette as a control. shRNA-expressing cells were selected with puromycin, and two constructs (B and D) were examined for Panx1 knockdown (KD).

Techniques: Inhibition, Expressing, Labeling, Western Blot, Positive Control, Incubation, Transfection, shRNA, Construct, SDS Page

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: ECM detachment causes a switch from glucose-to glutamine-dependent survival mechanisms. (A) Intracellular ATP levels in HepG2 cells 24 h after plating in adherent (AT) or non-adherent (poly-HEMA-coated) (DT) plates. (B–D) Changes in glucose, lactate, and glutamine concentration in the medium of HepG2 cells after 24 h under attached or detached conditions. Data are presented as mean ± SD of three independent experiments. Full-length PARP (F-PARP) and cleaved PARP (C-PARP) expression in protein extracts obtained from HepG2 cells incubated in the presence of (E) 50 μM UK5099 and (F) 1 μM antimycin A1 or oligomycin, or in their absence (Cont) for 24 h under attached or detached conditions. (G) F-PARP and C-PARP expression in protein extracts obtained from three different cancer cell lines (HepG2, HeLa, and HT1080) incubated with 25 mM 2DG, 20 μM 3PO, 1 mM GPNA, or 20 μM BPTES, or without these chemicals (Cont) for 24 h under attached or detached conditions. α-tubulin served as a loading control. Representative western blots are shown. * P < 0.05; ** P < 0.01.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Concentration Assay, Expressing, Incubation, Control, Western Blot

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: Glutamine is indispensable for cancer cell survival under ECM detachment. (A) ATP levels in HepG2, HeLa, and HT1080 cells cultured in complete medium, glucose-deficient (Glc (-)), glutamine-deficient (Gln (-)), or glucose and glutamine-deficient (Neither) medium for 24 h under attached (AT) or detached (DT) conditions. (B) Full-length PARP (F-PARP) and cleaved PARP (C-PARP) expression in HepG2 cells cultured as indicated in panel A for 24 h. β-actin served as a loading control. (C) Viability of HepG2 cells cultured for 24 h in the indicated medium on adherent or poly-HEMA-coated plates. (D) ATP levels in HepG2 cells cultured in the indicated nutrient-deficient or supplemented medium on attachment or detachment plates for 24 h. Complete: DMEM-based complete nutrient medium; AA: DMEM-amino acid; Vit: DMEM-vitamin; All deficient: deficient for all nutrients. (E) F-PARP and C-PARP expression in HepG2 cells cultured in the indicated nutrient-deficient or supplemented medium on attachment or detachment plates for 24 h. (F) F-PARP or C-PARP expression in HepG2 cells cultured in complete medium or in all nutrients-free medium supplemented with 2 mM glutamine and the indicated doses of cystine for 24 h under detached conditions. α-tubulin served as a loading control. (G) ROS (H 2 O 2 ) and (H) ATP levels in HepG2 cells cultured in complete medium or all nutrients-free medium supplemented with 2 mM glutamine and the indicated dose of cystine for 24 h in detached conditions. (I) H2AX phosphorylation (p-H2AX) and PARP expression in whole-cell extracts of HepG2 cells incubated with or without 1 mM BSO for 24 h under attached or detached conditions. β-actin served as a loading control. (J) ATP levels, (K) ROS levels, (L) H2AX phosphorylation and PARP expression in HepG2 cells cultured in glutamine-free medium in the presence (Cont) or absence (-) of glutamine, with or without 4 mM DM-αKG under detached conditions. β-actin served as a loading control. Representative western blots are shown. Data are presented as mean ± SD of three independent sets of experiments. NS, not significant; ** P < 0.01; *** P < 0.001.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Cell Culture, Expressing, Control, Phospho-proteomics, Incubation, Western Blot

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: AMPK is involved in glutamine metabolism upon ECM detachment. HepG2 cells stably expressing control-shRNA (sh-con) or AMPKα1-shRNA (sh-AMPK) were cultured in attachment (AT) or detachment (DT) dishes for 24 h. (A) Full-length PARP (F-PARP) and cleaved PARP (C-PARP), phosphorylated H2AX (p-H2AX) expression, and (C) ASCT2 expression in protein extracts of the above cells. β-actin served as a loading control. (B) Glutamine in culture medium and (D) intracellular ATP levels in the above cells. Representative western blots are shown. The expression levels of p-H2AX, C-PARP, and ASCT2 were measured by densitometric analysis. Data are presented as mean ± SD of three independent sets of experiments. NS, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Stable Transfection, Expressing, Control, shRNA, Cell Culture, Western Blot

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: Glutamine metabolism-mediated cancer cell survival is regulated by AMPK-Nrf2 under ECM detachment. (A, B, D, E) HepG2 cells expressing sh-con or sh-AMPK were cultured in attachment (AT) or poly-HEMA-coated (DT) dishes for 24 h. Western blot analysis was performed on protein extracts of these cells with antibodies against the indicated proteins, with either β-actin or lamin B1 as loading controls. (A, D) The asterisk indicates a nonspecific band. The expression levels of protein were measured by densitometric analysis. (C) Cells stably expressing sh-con were transfected with an empty vector. Cells stably expressing sh-AMPK were transfected with either an empty vector or the EGFP-Nrf2 expression vector. Western blot analysis was performed on protein extracts of these cell lines with antibodies against the indicated proteins after culturing in adherent or poly-HEMA-coated dishes for 24 h. Representative image of western blots are shown. (F) ROS levels in HepG2 cells stably expressing sh-con, sh-AMPK, or sh-Nrf2 for 24 h after plating in adherent or poly-HEMA-coated pates for 24 h. Data are presented as mean ± SD of three independent experiments. * P < 0.05; ** P < 0.01; *** P < 0.001.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Expressing, Cell Culture, Western Blot, Stable Transfection, Transfection, Plasmid Preparation

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: Loss of integrin regulates glutaminolysis in cancer cells. (A) Images obtained by phase-contrast microscopy of HepG2 cells cultured in the presence of different cilengitide (Cil) doses for 24 h in adherent culture dishes. Control cells were cultured using a poly-HEMA-coated dish without cilengitide treatment. Scale bar = 100 μm. (B) Western blot analysis of HepG2 cells treated with various doses (0–20 μM) of cilengitide for 24 h under attached conditions (unless otherwise indicated) and probed with antibodies against the indicated proteins, with either α-tubulin or lamin B1 as loading controls. (C) Full-length PARP (F-PARP) and cleaved PARP (C-PARP) expression in whole-cell lysates of HepG2 cells cultured in complete medium, glucose-free medium (Glc (-)), glutamine-free medium (Gln (-)), glucose- and glutamine-free medium (Neither), and the latter supplemented with either glucose (Glc (+)) or glutamine (Gln (+)) in the absence or presence of 20 μM cilengitide for 24 h. α-tubulin served as loading control. (D) ATP levels in HepG2 cells cultured in complete medium, glucose-deficient (Glc (-)), glutamine-deficient (Gln (-)), or glucose- and glutamine-deficient (Neither) medium in the presence of 20 μM cilengitide for 24 h. (E) F-PARP and C-PARP expression in whole-cell lysates of HepG2 cells cultured in glutamine-free medium (-) or control medium (+) for 24 h in the presence or absence of 20 μM cilengitide and 4 mM DM-αKG. α-tubulin served as loading control. (F–H) ATP levels and (I) F-PARP and C-PARP expression in HepG2 cells stably expressing sh-con, sh-AMPK, or sh-Nrf2 incubated in vehicle control medium (Cont) or glutamine-free medium (-) supplemented with 20 μM cilengitide for 24 h. β-actin served as a loading control. (J) ROS levels and (K) F-PARP and C-PARP expression in HepG2 cells treated or not with 20 μM BPTES or 10 μM CB839 in the presence of 20 μM cilengitide or in vehicle control medium (Cont) for 24 h. α-tubulin served as a loading control. Representative western blots are shown. Data are presented as mean ± SD of three independent experiments. * P < 0.05; ** P < 0.01.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Microscopy, Cell Culture, Control, Western Blot, Expressing, Stable Transfection, Incubation

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: A combination of sulfasalazine and CB839 causes cell damage by increasing oxidative stress in cancer cells following ECM detachment. (A) xCT expression in HepG2, HeLa, HT1080, and HaCaT cells cultured for 24 h under attached (AT) or detached (DT) conditions. β-actin served as loading control. The expression levels of xCT were measured by densitometric analysis. (B) Full-length PARP (F-PARP), cleaved PARP (C-PARP), and phosphorylated H2AX (p-H2AX) expression in HepG2 cells treated with various doses (0–500 μM) of sulfasalazine (SAS) for 24 h under attached or detached conditions. α-tubulin served as a loading control. (C) F-PARP, C-PARP, and p-H2AX expression and (D) ROS levels in HepG2 cells treated with either 10 μM CB839 or 250 μM sulfasalazine, or both. α-tubulin served as a loading control. Representative western blots are shown. Data are presented as mean ± SD of three independent experiments. * P < 0.05; ** P < 0.01.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Expressing, Cell Culture, Control, Western Blot

Journal: Redox Biology

Article Title: Metabolic reprogramming sustains cancer cell survival following extracellular matrix detachment

doi: 10.1016/j.redox.2020.101643

Figure Lengend Snippet: Cancer cells with high metastatic potential have an increased dependence on glutamine metabolism under detached conditions. (A, C) Full-length PARP (F-PARP), cleaved PARP (C-PARP), and phosphorylated H2AX (p-H2AX) expression in whole-cell lysates of A375P, A375-MA2, MCF-7, and MDA-MB-231 cells cultured in complete medium, glucose-deficient (Glc (-)), glutamine-deficient (Gln (-)), or glucose and glutamine-deficient (Neither) medium for 24 h under attached (AT) or detached (DT) conditions. (B, D) F-PARP, C-PARP, and p-H2AX expression in whole-cell lysates of HepG2 cells treated with either 10 μM CB839 or 250 μM sulfasalazine, or both for 24 h. α-tubulin served as loading control. Data are representative of three independent sets of experiments.

Article Snippet: Cells were obtained from the following sources: HeLa and HepG2 cells were purchased from JCRB (Osaka, Japan); BxPC-3, HT1080, and G361 cells were from ECACC (Salisbury, Scotland); A375-P, A375-MA2, and MDA-MB-231 cells were from ATCC (Manassas, VA, USA).

Techniques: Expressing, Cell Culture, Control