LATS2 is a tumor suppressor in a mouse lumB breast cancer model.

Slides:



Advertisements
Similar presentations
Normal skin tissue Supplementary Fig 1A KLF4 has a tumor suppressive function in human skin cancer. Skin cancer tissues were deparaffinized and IHC was.
Advertisements

Volume 14, Issue 10, Pages (March 2016)
SI-II A SI-II. Expression analysis of bladder cancer functionally active genes and significantly mutated genes. Comprehensive transcriptome profiling of.
Volume 19, Issue 5, Pages (May 2017)
Requirement for CDK4 kinase function in breast cancer
Volume 2, Issue 4, Pages (April 2008)
Klotho depletion increases MHC class II expression in the CP
Klotho reduction causes macrophage invasion into the CP
RNA-seq analysis of iWAT and eWAT.
Next-generation Sequencing Identifies Articular Cartilage and Subchondral Bone Mirnas after ESWT on Early Osteoarthritis Knee  C.-J. Wang, J.-H. Cheng,
(A) ZR75-1 cells were treated with 1 μM 5-aza-2′-deoxycytidine (5-Aza) for 4 d. (A) ZR75-1 cells were treated with 1 μM 5-aza-2′-deoxycytidine (5-Aza)
PPARγ signaling correlates with LATS2 in human and mouse tumors and promotes cell death in a LATS2-dependent manner. PPARγ signaling correlates with LATS2.
Sunitinib plus rMVA–CEA–TRICOM vaccine decreased tumor burden and increased intratumoral infiltration of T lymphocytes in the MC38-CEA colon carcinoma.
Combined PLX3397 and PTX treatment inhibits metastasis in a CD8-dependent manner. Combined PLX3397 and PTX treatment inhibits metastasis in a CD8-dependent.
Fig. 3. Obese IFN-γ−/− mice develop accelerated NAFLD with fibrosis.
High-throughput analysis of informative CpG sites for the four studied tumor suppressor genes (A-D). High-throughput analysis of informative CpG sites.
Regulation of Mammary Luminal Cell Fate and Tumorigenesis by p38α
Analysis of total and polysomal RNA clk-1(qm30) and clk-1(qm30)+WT.
(A) Schematic representation of the conditional Lats1 locus.
B7-H4 expression correlates with MHC-I expression and improved prognosis in patients with breast cancer. B7-H4 expression correlates with MHC-I expression.
Periostin Limits Tumor Response to VEGFA Inhibition
Deletion of Lats1 is phenotypically distinct from Lats2 deletion in PyMT tumors. Deletion of Lats1 is phenotypically distinct from Lats2 deletion in PyMT.
LATS2 promotes death of lumB cells.
Individual genes exhibit distinct female-enriched expression patterns.
Molecular Therapy - Nucleic Acids
(A) Genotyping of the Lats2 and Cre alleles in the PyMT-derived cell lines (see primers location in Fig S2A). (A) Genotyping of the Lats2 and Cre alleles.
Volume 14, Issue 10, Pages (March 2016)
BDNF expression in the cerebellum and brain stem region.
Down-regulation of LATS1 promotes the formation of tumors enriched in basal-like features. Down-regulation of LATS1 promotes the formation of tumors enriched.
Existence of a nuclear NFATc1–STAT3 complex in pancreatic cancer.
AZA treatment induces a distinct gene-expression pattern in stromal cells. AZA treatment induces a distinct gene-expression pattern in stromal cells. (A-C)
Volume 8, Issue 3, Pages (August 2014)
P2X4R blockade increases pro‐inflammatory gene expression after EAE
RNA-seq of the clk-1(qm30) (± nuclear or WT clk-1) mutants.
Volume 29, Issue 3, Pages (March 2016)
LATS2-associated gene expression pattern is down-regulated specifically in lumB breast tumors. LATS2-associated gene expression pattern is down-regulated.
Metascape Tripathi et al 2015pathways enrichment analysis (Tripathi et al 2015, of differentially expressed genes (counts > 5, FC.
(A) Schematic representation of the conditional Lats2 locus.
(A) Distribution of LATS2 mRNA expression levels in different breast cancer subtypes (PAM50, METABTIC dataset); ***P-value < 0.001, t test comparing lumB.
IL-10R-deficient macrophages secrete IL-23, inducing IL-22 secretion by ILC3 and TH17 cells. IL-10R-deficient macrophages secrete IL-23, inducing IL-22.
DDR1 plays an intrinsic role in primary epithelial cells undergoing branching morphogenesis and is required for correct organization of the basement membrane.
Comparison ofMyc-induced zebrafish liver tumors with different stages of human HCC and seven mouse HCC models. Comparison ofMyc-induced zebrafish liver.
(A) Western blot probing nuclear extract from wild-type (wt) and the newly generated ACF1 mutant (AcfC) embryos (0–16 h). (A) Western blot probing nuclear.
Extended analysis of differential expression datasets.
Whole-genome microarray analysis of gene expression in the livers of control mice and STAM mice subjected to NASH-derived hepatocarcinogenesis. Whole-genome.
(A) Relative expression levels of the top most down-regulated genes in LATS2L breast tumors (TCGA-BRCA dataset, see Fig 1) in the panel of breast cancer.
Chop deletion preserves β-cell function in P58IPK−/− mice.
Reduced OXPHOS expression and increased UCP expression.
MϕRIP140KD mice show browning in vWAT.
LATS2 augments oxidative phosphorylation.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
Fig. 5 Transcriptional changes in dKO mice after HFD regimen.
Loss of BAP1 blocks T cell differentiation at the DN3 stage in vitro.
Loss of RNA-Binding Protein Sfpq Causes Long-Gene Transcriptopathy in Skeletal Muscle and Severe Muscle Mass Reduction with Metabolic Myopathy  Motoyasu.
Volume 15, Issue 11, Pages (June 2016)
GC reaction is impaired in NOTCH2 knock-in mice.
Socially isolated SV40 Tag mice develop significantly larger mammary gland tumors. Socially isolated SV40 Tag mice develop significantly larger mammary.
Fig. 3 Transcriptional changes in dKO mice.
EMT gene expression patterns of M-Wnt and E-Wnt cells in vitro and in vivo. EMT gene expression patterns of M-Wnt and E-Wnt cells in vitro and in vivo.
MRNA expression IL-1α, IL-1β, IL-1Ra, IL-1RtI, ER α, ER β, and PR was analyzed by RT-PCR as described in “Materials and Methods.” Representative gel electrographies.
Example inverse FF-OCT images (left column) and corresponding histology images (right column) of ovarian metastases. Example inverse FF-OCT images (left.
Enrichment and detection of CTCs from orthotopic xenograft models of GBM. A, immunohistologic analysis of coronal sections showing mCherry expressing GBM8.
Expression of PCNA, K10, and K5 in skin lesions from Stat3+/−:HPV8 and Stat3+/+:HPV8 mice. Expression of PCNA, K10, and K5 in skin lesions from Stat3+/−:HPV8.
The CCR5+ population of SUM-159 cells is enriched with tumor-initiating cells. The CCR5+ population of SUM-159 cells is enriched with tumor-initiating.
Distinct subtypes of CAFs are detected in human PDAC
Gene expression heatmap of non–T-cell-inflamed, intermediate, and T-cell–inflamed testicular germ cell tumors from TCGA. Genes are on the row, and samples.
Transcriptomic Analysis of GmSIN1 OE-1 Transgenic Soybean.
Coculture with U937 cells enhances DNMT1 expression in gastric cancer cells. Coculture with U937 cells enhances DNMT1 expression in gastric cancer cells.
Genome-wide DNA hypomethylation associated with DNMT3A mutation in murine and human FLT3ITD AML. Human: A–C, volcano plot (A) representation of mean methylation.
Cxxc1-deficient TH17 cells exhibit a Treg cell–like expression profile
Presentation transcript:

LATS2 is a tumor suppressor in a mouse lumB breast cancer model. LATS2 is a tumor suppressor in a mouse lumB breast cancer model. (A) Relative total tumor weight, as percentage of total body weight of 3-mo-old Lats2-CKO PyMT and WT-PyMT littermate controls (n = number of mice); mean ± SEM; * P-value < 0.05. (B) Three mammary glands (see the Materials and Methods section) from Lats2-CKO PyMT and WT-PyMT littermate control mice were histologically scored. The most advanced pathological lesion from each mouse was tallied. (C) Representative H&E-stained sections from WT-PyMT (adenoma/MIN) and Lats2-CKO PyMT (carcinoma); scale bar = 500 μm. (D) Expression levels of Lats2 mRNA in WT-PyMT tumors of different histological stages, analyzed by RT-qPCR; mean ± SEM. (E) Left panel: Heatmap representing hierarchical clustering of global expression patterns of tumors from Lats2-CKO PyMT (n = 4) and WT-PyMT littermate controls (n = 3). Each tumor was taken from a different mouse. Standardized rld values are shown for differentially expressed genes (P-value < 0.05, n = 1131); ad = adenoma/MIN, car = carcinoma. Right panel: PCA of the most differentially expressed genes between Lats2-CKO PyMT and WT-PyMT tumors (adjP-value < 0.05), deduced from RNA-seq analysis. (F) GSEA of 1,131 genes ranked by fold change (red to blue gradient) between WT-PyMT and Lats2-CKO PyMT tumors (P-value < 0.05) and compared with genes down-regulated in LATS2L (versus LATSH) human lumB tumors (vertical black lines). Noa Furth et al. LSA 2018;1:e201800171 © 2018 Furth et al.