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: PLoS ONE

Article Title: Suppressor of Cytokine Signaling (SOCS) Genes Are Silenced by DNA Hypermethylation and Histone Deacetylation and Regulate Response to Radiotherapy in Cervical Cancer Cells

doi: 10.1371/journal.pone.0123133

Figure Lengend Snippet: Expression of SOCS1 (A), SOCS3 (B), and SOCS5 (C) gene were examined by qRT-PCR in normal cervix (N Cx) tissue, three normal fibroblast cell lines (CCD-18Co, CCD-18Lu, WI-38) and cervix cancer cell lines (CaSki, HeLa, ME-180, SiHa). Expression level of normal control samples marked as open bar and cervix cancer cell closed bar. Asterisk (*), statistically significant ( p <0.05).

Article Snippet: The human cervical carcinoma cell lines CaSki, HeLa, ME-180, and SiHa were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Expressing, Quantitative RT-PCR, Control

Journal: PLoS ONE

Article Title: Suppressor of Cytokine Signaling (SOCS) Genes Are Silenced by DNA Hypermethylation and Histone Deacetylation and Regulate Response to Radiotherapy in Cervical Cancer Cells

doi: 10.1371/journal.pone.0123133

Figure Lengend Snippet: CaSki (A,D), HeLa (B,E), and ME-180 (C,F) cells were treated with 10 μM of 5-Azacytosine (5-Aza) for 72 h (A-C) or infected with control lentivirus (shSCR) or lentivirus expressing shRNA targeting DNMT1 (shDNMT1) (D-F). Knock-down of DNMT1 and SOCS gene expression was examined with qRT-PCR. Asterisk (*), statistically significant ( p <0.05).

Article Snippet: The human cervical carcinoma cell lines CaSki, HeLa, ME-180, and SiHa were obtained from the Korean Cell Line Bank (KCLB, Seoul, Korea).

Techniques: Infection, Control, Expressing, shRNA, Knockdown, Gene Expression, Quantitative RT-PCR