Journal: Frontiers in Genetics

Article Title: Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing

doi: 10.3389/fgene.2021.798608

Figure Lengend Snippet: Nanopore sequencing found tandem HPV genomes in cervical cancer tissues and CaSki cells, respectively. (A) An 11.54 kb-long HPV 35 tandem genomic sequence was obtained by nanopore sequencing. The 11.54 kb-long sequence was aligned to HPV35 16B (NCBI: KX514416.1), which consists of three genomic segments, E1-E7-E6 (1567–10 nt), a whole genome frame (7894–10 nt), and URR-L1 (1561–10 nt. (B) A 21.18 kb-long HPV tandem sequence flanked with human genomic sequence at one end was obtained by nanopore sequencing from CaSki cells. The sequence was aligned to HPV16 (NCBI: U89348), in which a truncated genome (470–7905 nt) was connected to another truncated one (470–6905 nt) in a head-to-tail manner. (C) Another 15.07 kb-long HPV tandem sequence was obtained by nanopore sequencing from CaSki cells and was flanked at one end by the human gene; concatemers are formed by joining of incomplete HPV genomes with two spliced sites at 2032 nt and 4,586 nt.

Article Snippet: As a proof of concept, in this study, we completed whole genome sequencing from a cervical cancer tissue and a CaSki cell line with Oxford Nanopore Technologies.

Techniques: Nanopore Sequencing, Sequencing

Journal: Frontiers in Genetics

Article Title: Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing

doi: 10.3389/fgene.2021.798608

Figure Lengend Snippet: Physical state determination of the HPV genome by exonuclease V (ExoV)-qPCR–based assay.

Article Snippet: As a proof of concept, in this study, we completed whole genome sequencing from a cervical cancer tissue and a CaSki cell line with Oxford Nanopore Technologies.

Techniques:

Journal: Frontiers in Genetics

Article Title: Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing

doi: 10.3389/fgene.2021.798608

Figure Lengend Snippet: HPV integration sites identified by nanopore sequencing in CaSki cells and a cervical cancer tissue. (A) Distribution of HPV integration sites in different function regions of human genes identified from CaSki cells (HPV16) and a cervical cancer tissue (HPV35) by nanopore sequencing. (B) The HPV integration site was amplified by PCR from the CaSki cells, followed by agarose gel electrophoresis. C-33A cells (HPV-negative cervical cancer cells) was used as a negative control. (C) Sanger sequencing of the HPV integration site. PCR products were subjected to Sanger sequencing. Peaks of nucleotides at integration sites were shown. The cellular sequence from PRR30 was boxed with green color, and viral sequence was boxed with red color. (D) The sequence of the integration site located in PRR30 gene. The exon region of PRR30 gene was labeled with green color, and the URR region of HPV genome was labeled with red color. Three random nucleotides at the breakpoint (BP) were labeled with blue color.

Article Snippet: As a proof of concept, in this study, we completed whole genome sequencing from a cervical cancer tissue and a CaSki cell line with Oxford Nanopore Technologies.

Techniques: Nanopore Sequencing, Amplification, Agarose Gel Electrophoresis, Negative Control, Sequencing, Labeling

Journal: Cell Death & Disease

Article Title: Novel prosurvival function of Yip1A in human cervical cancer cells: constitutive activation of the IRE1 and PERK pathways of the unfolded protein response

doi: 10.1038/cddis.2017.147

Figure Lengend Snippet: Depletion of Yip1A induces apoptotic cell death in HeLa and CaSki cervical cancer cells. ( a ) HeLa and CaSki cells were transfected with control scramble siRNA (left panel) or Yip1A siRNA (right panel). Representative confocal micrographs show morphological differences between control and Yip1A-knockdown cells at the indicated time points. Scale bars are 50 μ m. ( b ) The viability of transfected cells was evaluated at the indicated time points using the MTT Cell Proliferation Assay. Data are means±S.D. from three independent experiments; * P <0.05, ** P <0.01. ( c ) Representative flow cytometric data for control (left panels) and Yip1A-knockdown (right panels) cells at the indicated time points after siRNA transfection. The percentages of apoptotic cells (Annexin V + /PI − + Annexin V + /PI + ) are shown in the bar graphs. Data are means±S.D. from three independent experiments; * P <0.05. ( d ) Representative confocal micrographs of control (upper panels) and Yip1A-knockdown (lower panels) cells at the indicated time points after siRNA transfection. Scale bars are 10 μ m. The percentages of TUNEL-positive cells are shown in the bar graphs. Data are means±S.D. from three independent experiments; * P <0.05, ** P <0.01. ( e ) Western blotting shows relative levels of cleaved caspase 3 and cleaved PARP protein in control and Yip1A-knockdown cells at the indicated time points after siRNA transfection. GAPDH was used for normalization. Data are means±S.D. from three independent experiments; * P <0.05, ** P <0.01

Article Snippet: A human cervical cancer cell line CaSki (IFO50007) was obtained from the Japanese Collection of Research Bioresources (JCRB, Osaka, Japan), and grown in RPMI 1640 Medium (Nissui) supplemented with 10% FBS (Sigma-Aldrich) and 2 mM l -glutamine (Gibco) under conditions of 5% CO 2 atmosphere at 37 °C.

Techniques: Transfection, Control, Knockdown, MTT Cell Proliferation, TUNEL Assay, Western Blot

Journal: Cell Death & Disease

Article Title: Novel prosurvival function of Yip1A in human cervical cancer cells: constitutive activation of the IRE1 and PERK pathways of the unfolded protein response

doi: 10.1038/cddis.2017.147

Figure Lengend Snippet: Schematic representation of how Yip1A operates as a prosurvival modulator that coordinately activates the IRE1 and PERK pathways of the UPR to support the survival of HeLa and CaSki cervical cancer cells. See text for details. Ub, ubiquitination

Article Snippet: A human cervical cancer cell line CaSki (IFO50007) was obtained from the Japanese Collection of Research Bioresources (JCRB, Osaka, Japan), and grown in RPMI 1640 Medium (Nissui) supplemented with 10% FBS (Sigma-Aldrich) and 2 mM l -glutamine (Gibco) under conditions of 5% CO 2 atmosphere at 37 °C.

Techniques: Ubiquitin Proteomics

Journal: Scientific Reports

Article Title: miR-193a-5p–mediated Inhibition of the METTL1/COX-2 axis is critical for Astragalin-induced apoptosis in cervical cancer

doi: 10.1038/s41598-025-32320-3

Figure Lengend Snippet: Effect of Astragalin on cytotoxicity in cervical cancer cells. ( A ) Chemical structure of Astragalin. Molecular weight = 448.38 g/mol ( B ) SiHa, Caski and Hela cells were seeded onto 96 well microplates and treated with various concentrations of Astragalin (0, 5, 10, 20 and 40 µM) for 24 h. Cell viability was evaluated by MTT assay. Data represent means ± SD. * p < 0.05, ** p < 0.01, *** p < 0.001versus untreated control. Experiments were performed in triplicate and repeated.

Article Snippet: Human SiHa, CaSki, and HeLa cervical cancer cell lines were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Molecular Weight, MTT Assay, Control

Journal: Scientific Reports

Article Title: miR-193a-5p–mediated Inhibition of the METTL1/COX-2 axis is critical for Astragalin-induced apoptosis in cervical cancer

doi: 10.1038/s41598-025-32320-3

Figure Lengend Snippet: Effect of Astragalin on apoptosis in SiHa and Caski cells. ( A ) SiHa and Caski cells were treated with Astragalin (0, 50 or 70 µM) for 24 h. The treated cells were fixed with 70% ethanol, stained with propidium iodide and analyzed by flow cytometry. ( B ) SiHa and Caski cells were treated with Astragalin (0, 10 or 20 µM) for 24 h. Cell lysates were prepared and subjected to Western blotting for pro- PARP, procaspase-3 and cleaved caspase-3. Experiments were performed in triplicate and repeated.

Article Snippet: Human SiHa, CaSki, and HeLa cervical cancer cell lines were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Staining, Flow Cytometry, Western Blot

Journal: Scientific Reports

Article Title: miR-193a-5p–mediated Inhibition of the METTL1/COX-2 axis is critical for Astragalin-induced apoptosis in cervical cancer

doi: 10.1038/s41598-025-32320-3

Figure Lengend Snippet: Survival rate of METTL1 overexpression and effect of Astragalin on METTL1 and Cox2 in SiHa and Caski cells. ( A ) METTL1 mRNA level in tissues of normal and cervical cancer patients by TCGA analysis. ( B ) Effect of METTL1 on the survival rate in the patients with cervical cancer cells. ( C ) SiHa and Caski cells were treated with Astragalin for 24 h. Cell lysates were prepared and subjected to Western blotting for METTL1 and COX-2. Experiments were performed in triplicate and repeated.

Article Snippet: Human SiHa, CaSki, and HeLa cervical cancer cell lines were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Over Expression, Western Blot

Journal: Scientific Reports

Article Title: miR-193a-5p–mediated Inhibition of the METTL1/COX-2 axis is critical for Astragalin-induced apoptosis in cervical cancer

doi: 10.1038/s41598-025-32320-3

Figure Lengend Snippet: Effect of Astragalin on METTL1 and Cox2 stability in SiHa and Caski cells. Cells were treated with Astragalin (70 µM) for 24 h, exposed to 50 µg/ml cycloheximide for the indicated time (0, 120 and 240 min) and subjected to Western blotting with antibodies of METTL1 and Cox2. Experiments were performed in triplicate and repeated.

Article Snippet: Human SiHa, CaSki, and HeLa cervical cancer cell lines were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Western Blot

Journal: Scientific Reports

Article Title: miR-193a-5p–mediated Inhibition of the METTL1/COX-2 axis is critical for Astragalin-induced apoptosis in cervical cancer

doi: 10.1038/s41598-025-32320-3

Figure Lengend Snippet: Effect of Astragalin on interaction between METTL1 and Cox2 in SiHa and Caski cells. ( A ) RNA-seq data (cBioportal) confirms a strong correlation between METTL1 and Cox2 with Spearman correlation of 0.16. ( B ) SiHa and Caski cells were treated with Astragalin for 24 h and Immunoprecipitation (IP) was performed with lysates and also Western blot analysis was conducted to detect METTL1 and Cox2 in whole cell lysates. ( C ) mRNA expression levels of METTL1 and Cox2 were measured in SiHa cells treated with siRNA and/or Astragalin. ( D ) Effect of METTL1 overexpression on METTL1 and Cox2 in Astragalin treated SiHa cells. ( E ) Effect of METTL1 depletion on METTL1 and Cox2 in Astraglain treated SiHa cells. Experiments were performed in triplicate and repeated.

Article Snippet: Human SiHa, CaSki, and HeLa cervical cancer cell lines were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: RNA Sequencing, Immunoprecipitation, Western Blot, Expressing, Over Expression