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Gene: MMP14 |
Gene summary for MMP14 |
Gene summary. |
Gene information | Species | Human | Gene symbol | MMP14 | Gene ID | 4323 |
Gene name | matrix metallopeptidase 14 | |
Gene Alias | MMP-14 | |
Cytomap | 14q11.2 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | P50281 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4323 | MMP14 | LZE2T | Human | Esophagus | ESCC | 5.56e-03 | 4.30e-01 | 0.082 |
4323 | MMP14 | LZE4T | Human | Esophagus | ESCC | 1.19e-11 | 5.76e-01 | 0.0811 |
4323 | MMP14 | LZE5T | Human | Esophagus | ESCC | 1.80e-04 | 2.44e-01 | 0.0514 |
4323 | MMP14 | LZE8T | Human | Esophagus | ESCC | 1.21e-05 | 2.94e-01 | 0.067 |
4323 | MMP14 | LZE22D1 | Human | Esophagus | HGIN | 3.39e-02 | -2.12e-02 | 0.0595 |
4323 | MMP14 | LZE22T | Human | Esophagus | ESCC | 1.15e-10 | 2.68e-01 | 0.068 |
4323 | MMP14 | LZE24T | Human | Esophagus | ESCC | 5.98e-12 | 3.45e-01 | 0.0596 |
4323 | MMP14 | P2T-E | Human | Esophagus | ESCC | 7.68e-28 | 7.48e-01 | 0.1177 |
4323 | MMP14 | P4T-E | Human | Esophagus | ESCC | 2.18e-24 | 1.03e+00 | 0.1323 |
4323 | MMP14 | P5T-E | Human | Esophagus | ESCC | 3.37e-21 | 7.76e-01 | 0.1327 |
4323 | MMP14 | P8T-E | Human | Esophagus | ESCC | 7.91e-22 | 5.82e-01 | 0.0889 |
4323 | MMP14 | P9T-E | Human | Esophagus | ESCC | 3.01e-18 | 8.26e-01 | 0.1131 |
4323 | MMP14 | P10T-E | Human | Esophagus | ESCC | 1.43e-56 | 1.48e+00 | 0.116 |
4323 | MMP14 | P11T-E | Human | Esophagus | ESCC | 4.71e-34 | 1.89e+00 | 0.1426 |
4323 | MMP14 | P12T-E | Human | Esophagus | ESCC | 1.19e-60 | 1.50e+00 | 0.1122 |
4323 | MMP14 | P15T-E | Human | Esophagus | ESCC | 2.83e-58 | 1.90e+00 | 0.1149 |
4323 | MMP14 | P16T-E | Human | Esophagus | ESCC | 1.92e-32 | 7.07e-01 | 0.1153 |
4323 | MMP14 | P17T-E | Human | Esophagus | ESCC | 1.33e-07 | 8.85e-01 | 0.1278 |
4323 | MMP14 | P19T-E | Human | Esophagus | ESCC | 9.37e-12 | 2.02e+00 | 0.1662 |
4323 | MMP14 | P20T-E | Human | Esophagus | ESCC | 2.43e-14 | 4.27e-01 | 0.1124 |
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Transcriptomic changes along malignancy continuum. |
∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | |
Colorectum | SER | |
Colorectum | MSS | |
Colorectum | MSI-H | |
Colorectum | FAP |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00614585 | Liver | Cirrhotic | reproductive system development | 132/4634 | 427/18723 | 2.07e-03 | 1.28e-02 | 132 |
GO:00486085 | Liver | Cirrhotic | reproductive structure development | 131/4634 | 424/18723 | 2.19e-03 | 1.34e-02 | 131 |
GO:0043627 | Liver | Cirrhotic | response to estrogen | 30/4634 | 75/18723 | 2.52e-03 | 1.51e-02 | 30 |
GO:00487711 | Liver | Cirrhotic | tissue remodeling | 60/4634 | 175/18723 | 2.86e-03 | 1.65e-02 | 60 |
GO:1905523 | Liver | Cirrhotic | positive regulation of macrophage migration | 13/4634 | 26/18723 | 4.72e-03 | 2.48e-02 | 13 |
GO:0070613 | Liver | Cirrhotic | regulation of protein processing | 26/4634 | 65/18723 | 4.73e-03 | 2.48e-02 | 26 |
GO:00605411 | Liver | Cirrhotic | respiratory system development | 67/4634 | 203/18723 | 4.81e-03 | 2.52e-02 | 67 |
GO:00026876 | Liver | Cirrhotic | positive regulation of leukocyte migration | 47/4634 | 135/18723 | 5.55e-03 | 2.81e-02 | 47 |
GO:0007492 | Liver | Cirrhotic | endoderm development | 29/4634 | 77/18723 | 8.02e-03 | 3.76e-02 | 29 |
GO:00071624 | Liver | Cirrhotic | negative regulation of cell adhesion | 93/4634 | 303/18723 | 1.06e-02 | 4.66e-02 | 93 |
GO:002241112 | Liver | HCC | cellular component disassembly | 282/7958 | 443/18723 | 1.02e-19 | 1.38e-17 | 282 |
GO:000697922 | Liver | HCC | response to oxidative stress | 281/7958 | 446/18723 | 9.75e-19 | 1.24e-16 | 281 |
GO:004586222 | Liver | HCC | positive regulation of proteolysis | 232/7958 | 372/18723 | 5.66e-15 | 3.98e-13 | 232 |
GO:007265921 | Liver | HCC | protein localization to plasma membrane | 177/7958 | 284/18723 | 1.02e-11 | 4.18e-10 | 177 |
GO:199077821 | Liver | HCC | protein localization to cell periphery | 200/7958 | 333/18723 | 6.07e-11 | 2.23e-09 | 200 |
GO:001604921 | Liver | HCC | cell growth | 269/7958 | 482/18723 | 1.84e-09 | 5.35e-08 | 269 |
GO:190547511 | Liver | HCC | regulation of protein localization to membrane | 113/7958 | 175/18723 | 2.90e-09 | 7.78e-08 | 113 |
GO:005160412 | Liver | HCC | protein maturation | 171/7958 | 294/18723 | 3.80e-08 | 8.30e-07 | 171 |
GO:190437521 | Liver | HCC | regulation of protein localization to cell periphery | 83/7958 | 125/18723 | 5.60e-08 | 1.19e-06 | 83 |
GO:000155821 | Liver | HCC | regulation of cell growth | 228/7958 | 414/18723 | 1.34e-07 | 2.55e-06 | 228 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0466810 | Esophagus | ESCC | TNF signaling pathway | 89/4205 | 114/8465 | 3.36e-10 | 4.01e-09 | 2.06e-09 | 89 |
hsa0492816 | Esophagus | ESCC | Parathyroid hormone synthesis, secretion and action | 66/4205 | 106/8465 | 5.86e-03 | 1.47e-02 | 7.51e-03 | 66 |
hsa0466817 | Esophagus | ESCC | TNF signaling pathway | 89/4205 | 114/8465 | 3.36e-10 | 4.01e-09 | 2.06e-09 | 89 |
hsa0492817 | Esophagus | ESCC | Parathyroid hormone synthesis, secretion and action | 66/4205 | 106/8465 | 5.86e-03 | 1.47e-02 | 7.51e-03 | 66 |
hsa046684 | Liver | HCC | TNF signaling pathway | 73/4020 | 114/8465 | 2.53e-04 | 1.19e-03 | 6.63e-04 | 73 |
hsa0466811 | Liver | HCC | TNF signaling pathway | 73/4020 | 114/8465 | 2.53e-04 | 1.19e-03 | 6.63e-04 | 73 |
hsa046689 | Oral cavity | OSCC | TNF signaling pathway | 82/3704 | 114/8465 | 8.30e-10 | 9.59e-09 | 4.88e-09 | 82 |
hsa0466816 | Oral cavity | OSCC | TNF signaling pathway | 82/3704 | 114/8465 | 8.30e-10 | 9.59e-09 | 4.88e-09 | 82 |
hsa0466822 | Oral cavity | LP | TNF signaling pathway | 49/2418 | 114/8465 | 6.51e-04 | 3.29e-03 | 2.12e-03 | 49 |
hsa0466832 | Oral cavity | LP | TNF signaling pathway | 49/2418 | 114/8465 | 6.51e-04 | 3.29e-03 | 2.12e-03 | 49 |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
Annotation of somatic variants for genes involved in malignant transformation |
Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
MMP14 | SNV | Missense_Mutation | c.679N>A | p.Asp227Asn | p.D227N | P50281 | protein_coding | tolerated(0.88) | benign(0.015) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MMP14 | SNV | Missense_Mutation | rs774971754 | c.1027C>T | p.Arg343Trp | p.R343W | P50281 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AC-A5XU-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | letrozole | SD |
MMP14 | SNV | Missense_Mutation | c.1369G>A | p.Glu457Lys | p.E457K | P50281 | protein_coding | tolerated(1) | benign(0.003) | TCGA-AR-A1AP-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | anastrozole | SD | |
MMP14 | SNV | Missense_Mutation | c.384C>G | p.Ile128Met | p.I128M | P50281 | protein_coding | deleterious(0) | probably_damaging(0.975) | TCGA-D8-A1JC-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD | |
MMP14 | SNV | Missense_Mutation | rs770606883 | c.1186G>A | p.Glu396Lys | p.E396K | P50281 | protein_coding | deleterious(0.02) | possibly_damaging(0.806) | TCGA-VS-A9UR-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
MMP14 | SNV | Missense_Mutation | rs748601843 | c.445N>T | p.Arg149Cys | p.R149C | P50281 | protein_coding | deleterious(0.03) | possibly_damaging(0.832) | TCGA-A6-A565-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unspecific | 5FU | PD |
MMP14 | SNV | Missense_Mutation | c.790N>G | p.Met264Val | p.M264V | P50281 | protein_coding | deleterious(0.03) | benign(0.382) | TCGA-AA-3966-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MMP14 | SNV | Missense_Mutation | c.433C>T | p.Arg145Cys | p.R145C | P50281 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
MMP14 | SNV | Missense_Mutation | c.5N>A | p.Ser2Tyr | p.S2Y | P50281 | protein_coding | tolerated_low_confidence(0.06) | benign(0) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
MMP14 | SNV | Missense_Mutation | rs758484236 | c.1607C>T | p.Ala536Val | p.A536V | P50281 | protein_coding | tolerated(0.21) | benign(0.012) | TCGA-EI-6507-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | inhibitor | 252166779 | ||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | inhibitor | 252827503 | CGS-27023A | |
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | CARMINIC ACID | CARMINIC ACID | ||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | inhibitor | 178103981 | ILOMASTAT | |
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | vaccine | PRINOMASTAT | PRINOMASTAT | |
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | Epigallocatechin gallate | |||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | BT-1718 | |||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | inhibitor | 405560328 | ||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | PYROGALLOL RED | PYROGALLOL RED | ||
4323 | MMP14 | PROTEASE, DRUGGABLE GENOME, ENZYME | GM6001 |
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