cervical squamous cell carcinoma |
Disease ID | 1090 |
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Disease | cervical squamous cell carcinoma |
Definition | A squamous cell carcinoma arising from the cervical epithelium. It usually evolves from a precancerous cervical lesion. Increased numbers of sexual partners and human papillomavirus (HPV) infection are risk factors for cervical squamous cell carcinoma. The following histologic patterns have been described: conventional squamous cell carcinoma, papillary squamous cell carcinoma, transitional cell carcinoma, lymphoepithelioma-like carcinoma, verrucous carcinoma, condylomatous carcinoma and spindle cell carcinoma. Survival is most closely related to the stage of disease at the time of diagnosis. |
Synonym | cancer cell cervix squamous cancer cells cervix squamous cancer of the cervix, squamous cell carcinoma cell cervix squamous carcinoma of the cervix, squamous cell cervical cancer, squamous cell carcinoma cervical epidermoid carcinoma cervical squamous cell carcinoma, nos cervical squamous cell carcinoma, not otherwise specified cervix cancer, squamous cell carcinoma cervix squamous cell carcinoma cervix uteri squamous cell carcinoma epidermoid carcinoma of the cervix squamous cell cancer of the cervix squamous cell carcinoma cervical squamous cell carcinoma cervix squamous cell carcinoma of cervix squamous cell carcinoma of cervix (disorder) squamous cell carcinoma of cervix uteri squamous cell carcinoma of the cervix squamous cell carcinoma of the cervix uteri squamous cell carcinoma of the uterine cervix squamous cell carcinoma of uterine cervix squamous cervical cancer uterine cervical cancer, squamous cell carcinoma uterine cervix cancer, squamous cell carcinoma uterine cervix squamous cell carcinoma |
Orphanet | |
DOID | |
UMLS | C0279671 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:11) C0007137 | squamous cell carcinoma | 64 C0279671 | squamous cell carcinoma of the cervix | 48 C0279671 | squamous cell carcinoma of the uterine cervix | 20 C0011633 | dermatomyositis | 1 C0007134 | renal cell carcinomas | 1 C0007134 | renal cell carcinoma | 1 C0279671 | squamous cell cancer of the cervix | 1 C0002871 | anemia | 1 C0206623 | adenosquamous cell carcinoma | 1 C0279671 | squamous cell carcinoma of uterine cervix | 1 C0007137 | squamous cell cancer | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:3) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:96) 37 | ACADVL | 1.115 | DISEASES 51309 | ARMCX1 | 3.24 | DISEASES 51374 | ATRAID | 3.431 | DISEASES 554 | AVPR2 | 1.157 | DISEASES 9531 | BAG3 | 1.046 | DISEASES 578 | BAK1 | 1.134 | DISEASES 8678 | BECN1 | 1.545 | DISEASES 676 | BRDT | 1.952 | DISEASES 682 | BSG | 1.157 | DISEASES 900 | CCNG1 | 1.509 | DISEASES 960 | CD44 | 1.005 | DISEASES 1029 | CDKN2A | 3.355 | DISEASES 1164 | CKS2 | 1.838 | DISEASES 54544 | CRCT1 | 3.105 | DISEASES 1499 | CTNNB1 | 2.532 | DISEASES 9547 | CXCL14 | 1.016 | DISEASES 23234 | DNAJC9 | 3.042 | DISEASES 29102 | DROSHA | 1.969 | DISEASES 1855 | DVL1 | 1.223 | DISEASES 1915 | EEF1A1 | 1.099 | DISEASES 83481 | EPPK1 | 2.552 | DISEASES 2195 | FAT1 | 1.001 | DISEASES 2263 | FGFR2 | 1.516 | DISEASES 2272 | FHIT | 2.138 | DISEASES 2805 | GOT1 | 1.698 | DISEASES 3068 | HDGF | 1.445 | DISEASES 3123 | HLA-DRB1 | 2.107 | DISEASES 8519 | IFITM1 | 1.377 | DISEASES 3594 | IL12RB1 | 1.164 | DISEASES 83737 | ITCH | 1.733 | DISEASES 3655 | ITGA6 | 1.917 | DISEASES 3710 | ITPR3 | 1.253 | DISEASES 3745 | KCNB1 | 1.282 | DISEASES 81033 | KCNH6 | 2.269 | DISEASES 10112 | KIF20A | 2.056 | DISEASES 688 | KLF5 | 1.142 | DISEASES 113730 | KLHDC7B | 3.622 | DISEASES 5650 | KLK7 | 1.098 | DISEASES 3880 | KRT19 | 1.935 | DISEASES 3855 | KRT7 | 1.743 | DISEASES 3914 | LAMB3 | 2.158 | DISEASES 3965 | LGALS9 | 1.153 | DISEASES 3981 | LIG4 | 1.369 | DISEASES 348120 | LINC01193 | 1.734 | DISEASES 121227 | LRIG3 | 2.381 | DISEASES 23542 | MAPK8IP2 | 3.263 | DISEASES 10747 | MASP2 | 1.307 | DISEASES 4149 | MAX | 1.848 | DISEASES 27030 | MLH3 | 1.568 | DISEASES 64710 | NUCKS1 | 2.255 | DISEASES 11240 | PADI2 | 1.385 | DISEASES 5094 | PCBP2 | 1.867 | DISEASES 10401 | PIAS3 | 1.447 | DISEASES 5580 | PRKCD | 1.648 | DISEASES 5696 | PSMB8 | 1.049 | DISEASES 5743 | PTGS2 | 1.238 | DISEASES 22827 | PUF60 | 2.154 | DISEASES 83871 | RAB34 | 2.002 | DISEASES 5890 | RAD51B | 1.389 | DISEASES 5893 | RAD52 | 1.298 | DISEASES 2889 | RAPGEF1 | 1.172 | DISEASES 5915 | RARB | 1.661 | DISEASES 11186 | RASSF1 | 1.627 | DISEASES 51634 | RBMX2 | 3.281 | DISEASES 5996 | RGS1 | 1.495 | DISEASES 54101 | RIPK4 | 2.075 | DISEASES 6239 | RREB1 | 1.68 | DISEASES 57142 | RTN4 | 1.227 | DISEASES 6304 | SATB1 | 1.232 | DISEASES 286205 | SCAI | 1.445 | DISEASES 6318 | SERPINB4 | 2.435 | DISEASES 23451 | SF3B1 | 2.112 | DISEASES 6424 | SFRP4 | 2.041 | DISEASES 6477 | SIAH1 | 1.375 | DISEASES 9058 | SLC13A2 | 2.047 | DISEASES 284111 | SLC13A5 | 2.053 | DISEASES 6622 | SNCA | 1.292 | DISEASES 6657 | SOX2 | 2.098 | DISEASES 6696 | SPP1 | 1.387 | DISEASES 10388 | SYCP2 | 2.938 | DISEASES 23345 | SYNE1 | 1.301 | DISEASES 161176 | SYNE3 | 3.154 | DISEASES 8407 | TAGLN2 | 3.243 | DISEASES 6892 | TAPBP | 1.171 | DISEASES 6942 | TCF20 | 1.569 | DISEASES 84260 | TCHP | 1.027 | DISEASES 7012 | TERC | 1.002 | DISEASES 200424 | TET3 | 1.828 | DISEASES 56649 | TMPRSS4 | 1.546 | DISEASES 5987 | TRIM27 | 1.9 | DISEASES 7204 | TRIO | 2.062 | DISEASES 55503 | TRPV6 | 1.168 | DISEASES 117581 | TWIST2 | 1.319 | DISEASES 10537 | UBD | 1.499 | DISEASES 7422 | VEGFA | 1.3 | DISEASES 6935 | ZEB1 | 1.178 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1090 |
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Disease | cervical squamous cell carcinoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:8) HP:0002860 | Squamous cell carcinoma | 73 HP:0002664 | Neoplasia | 2 HP:0000125 | Pelvic kidney | 1 HP:0012531 | Pain | 1 HP:0002840 | Lymphadenitis | 1 HP:0002835 | Aspiration | 1 HP:0005584 | Renal cell carcinoma | 1 HP:0001903 | Anemia | 1 |
Disease ID | 1090 |
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Disease | cervical squamous cell carcinoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:6) |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:8) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs2229546 | 23280621 | 3587 | IL10RA | umls:C0279671 | BeFree | Cervical SCC risk was associated with the minor alleles of the IL10RA rs9610 3' UTR SNP (OR=1.76, 95% CI=1.15-2.68) and two synonymous IL12RB2 SNPs (rs4297265, OR=0.46, 95% CI=0.26-0.82; rs2229546, OR=0.43, 95% CI=0.21-0.87). | 0.000271442 | 2013 | IL12RB2 | 1 | 67395837 | C | A,G,T |
rs3087386 | 18470628 | 51455 | REV1 | umls:C0279671 | BeFree | Compared with the REV1 Phe257Ser, women carrying Ser257Ser and Phe257Ser genotypes had a significantly decreased the risk for cervical carcinoma or cervical squamous cell carcinoma. | 0.000271442 | 2008 | REV1 | 2 | 99439044 | A | G |
rs3181224 | 23280621 | 3593 | IL12B | umls:C0279671 | BeFree | Finally, the minor allele of the IL12B rs3181224 3' UTR SNP was associated with a reduced risk of vulvar SCC (OR=0.30, 95% CI=0.12-0.74). | 0.000271442 | 2013 | LOC105377683 | 5 | 159313842 | A | G |
rs4297265 | 23280621 | 3587 | IL10RA | umls:C0279671 | BeFree | Cervical SCC risk was associated with the minor alleles of the IL10RA rs9610 3' UTR SNP (OR=1.76, 95% CI=1.15-2.68) and two synonymous IL12RB2 SNPs (rs4297265, OR=0.46, 95% CI=0.26-0.82; rs2229546, OR=0.43, 95% CI=0.21-0.87). | 0.000271442 | 2013 | NA | NA | NA | NA | NA |
rs4705343 | 26252302 | 3845 | KRAS | umls:C0279671 | BeFree | These findings indicate that miR-143/145 rs4705343 and KRAS rs712 may contribute to the etiology of CSCC in Chinese women. | 0.000542884 | 2015 | MIR143;MIR143HG | 5 | 149428518 | T | C |
rs712 | 26252302 | 3845 | KRAS | umls:C0279671 | BeFree | These findings indicate that miR-143/145 rs4705343 and KRAS rs712 may contribute to the etiology of CSCC in Chinese women. | 0.000542884 | 2015 | KRAS | 12 | 25209618 | A | C |
rs9298814 | 12490311 | 3451 | IFNA17 | umls:C0279671 | BeFree | The distribution of IFNA17 Ile184Arg genotype among SCCA cases (Ile/Ile, 21%; Arg/Ile, 57%; and Arg/Arg, 22%) was different significantly from that among NCC (Ile/Ile, 32%; Arg/Ile, 56%; and Arg/Arg, 12%) (P=0.0345). | 0.000271442 | 2003 | IFNA17 | 9 | 21227623 | A | G,C |
rs9610 | 23280621 | 3587 | IL10RA | umls:C0279671 | BeFree | Cervical SCC risk was associated with the minor alleles of the IL10RA rs9610 3' UTR SNP (OR=1.76, 95% CI=1.15-2.68) and two synonymous IL12RB2 SNPs (rs4297265, OR=0.46, 95% CI=0.26-0.82; rs2229546, OR=0.43, 95% CI=0.21-0.87). | 0.000271442 | 2013 | IL10RA | 11 | 118001371 | G | A |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 1090 |
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Disease | cervical squamous cell carcinoma |
Case | (Waiting for update.) |