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Image Search Results
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: Overexpressed PTK7 expression connected with poor prognosis. (a) Low and high PTK7 protein expressions in the tumor tissues by IHC were shown. (b) The negative PTK7 protein expression in the paired tumor-adjacent tissues by IHC. (c) The overall survival and progression-free survival in our clinical cohort: the high PTK7 protein expression level group was significantly associated with shorter progression-free survival compared to the low expression group ( ∗ P < 0.05, respectively).
Article Snippet: Human predesigned targeted short
Techniques: Expressing
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: Relationships of PTK7 and clinicopathological characteristics in 85 patients with cervical cancer.
Article Snippet: Human predesigned targeted short
Techniques: Expressing
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: Establishing the stable knockdown of PTK7 cell lines: (a, b) qRT-PCR and Western blot assay. PTK7 mRNA and protein levels were significantly decreased compared to the control. ( ∗ P < 0.05).
Article Snippet: Human predesigned targeted short
Techniques: Knockdown, Quantitative RT-PCR, Western Blot, Control
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: PTK7 regulated cell proliferation by Ki67 and PCNA proteins. (a) Colony formation assay. Results demonstrated that in Caski and SiHa cell lines, the control groups showed significantly higher survival fraction than the PTK7 knockdown groups ( ∗ P < 0.05). (b) MTT proliferation assay. OD values were showed to be significantly lower in the PTK7 knockdown group compared to control groups ( ∗ P < 0.05). (c, d) Western blot assay showed that the Ki67 and PCNA proteins were significantly downregulated in the PTK7 knockdown group compared to the control ( ∗ P < 0.05).
Article Snippet: Human predesigned targeted short
Techniques: Colony Assay, Control, Knockdown, Proliferation Assay, Western Blot
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: The role of PTK7 in cell migration and invasion in cervical cancer. (a) Cell scratch assay. The PTK7 knockdown group showed to have a great scratch gap in both two cervical cancer cell lines than control groups, respectively ( ∗ P < 0.05). (b) Cell invasion assay. The number of invasive cells in PTK7 knockdown groups was significantly lower than the control groups ( ∗ P < 0.05). (c, d) Western blot assay showed that MMP2 and MMP9 proteins were significantly downregulated in the PTK7 knockdown group compared to the control ( ∗ P < 0.05).
Article Snippet: Human predesigned targeted short
Techniques: Migration, Wound Healing Assay, Knockdown, Control, Invasion Assay, Western Blot
Journal: Disease Markers
Article Title: The Increased PTK7 Expression Is a Malignant Factor in Cervical Cancer
doi: 10.1155/2019/5380197
Figure Lengend Snippet: PTK7-depleted cells inhibit cervical cancer growth in vivo. (a, b) Xenograft assay. The tumor volume of the PTK7 knockdown group was significantly smaller than that of the control, after 4 weeks of management ( ∗ P < 0.05). (c, d) PTK7 protein level was dramatically decreased in the PTK7 knockdown group of injected tumor xenografts in nude mice by IHC and Western blot assays ( ∗ P < 0.05).
Article Snippet: Human predesigned targeted short
Techniques: In Vivo, Xenograft Assay, Knockdown, Control, Injection, Western Blot
Journal: Development (Cambridge, England)
Article Title: The L6 domain tetraspanin Tm4sf4 regulates endocrine pancreas differentiation and directed cell migration
doi: 10.1242/dev.058693
Figure Lengend Snippet: Tm4f4 disrupts actin organization and migration through a ROCK-independent Rho GTPase pathway. (A-I) F-actin localization and organization was analyzed by rhodamine phalloidin staining in NIH 3T3 fibroblast (A) and 293T fibroblast (B,C) cells expressing (arrows) or not expressing (arrowheads) Tm4sf4-FLAG, as well as in mPacL20 ductal epithelial cells transfected with control siRNA (D-F) or siTm4sf4 (G-I). Confocal magnification 63×. (J) Schematic depicting cytoskeletal actin structures (yellow) affected by Tm4sf4. (K) Percentage of mPacL20 cells exhibiting the phenotype displayed in G-I. (L,M) Nuclei positive cells migrated in Boyden chamber assays were compared in siControl (gray) and siTm4sf4 (black) transfected cells 16 hours after cells were treated with Rho family GTPase modulators. Error bars represent s.e.m. *P<0.05, **P<0.01.
Article Snippet: For siRNA knockdown, mPacL20 cells were transfected with 10 pmol
Techniques: Migration, Staining, Expressing, Transfection, Control