TSPAN31

gene
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Summary

TSPAN31 (tetraspanin 31, HGNC:10539) is a protein-coding gene on chromosome 12q14.1, encoding Tetraspanin-31 (Q12999).

The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is thought to be involved in growth-related cellular processes. This gene is associated with tumorigenesis and osteosarcoma.

Source: NCBI Gene 6302 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 178 total
  • MANE Select transcript: NM_005981

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:10539
Approved symbolTSPAN31
Nametetraspanin 31
Location12q14.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000135452
Ensembl biotypeprotein_coding
OMIM181035
Entrez6302

Gene structure

Transcript identifiers

Ensembl transcripts: 21 — 12 protein_coding, 4 protein_coding_CDS_not_defined, 3 retained_intron, 2 nonsense_mediated_decay

ENST00000257910, ENST00000546922, ENST00000546993, ENST00000547311, ENST00000547472, ENST00000547992, ENST00000548093, ENST00000548167, ENST00000549052, ENST00000550528, ENST00000550791, ENST00000552816, ENST00000553089, ENST00000553221, ENST00000870604, ENST00000870605, ENST00000870606, ENST00000870607, ENST00000918697, ENST00000918698, ENST00000958144

RefSeq mRNA: 3 — MANE Select: NM_005981 NM_001330168, NM_001330169, NM_005981

CCDS: CCDS86313, CCDS8952

Canonical transcript exons

ENST00000257910 — 6 exons

ExonStartEnd
ENSE000023356505774721657750219
ENSE000024182025774503957745217
ENSE000035554325774617657746256
ENSE000036234145774701857747131
ENSE000036837815774574557745912
ENSE000036901635774658957746720

Expression profiles

Bgee: expression breadth ubiquitous, 288 present calls, max score 97.62.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 22.7073 / max 1393.0810, expressed in 1800 samples.

FANTOM5 promoters (7 alternative TSS)

Promoter IDTPM avgSamples expressed
12632122.51161800
1263190.073321
1263180.054634
1263170.02718
1263150.02536
1263160.01024
2067550.00521

Top tissues by expression

295 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207997.62gold quality
islet of LangerhansUBERON:000000696.72gold quality
pericardiumUBERON:000240796.01gold quality
right lobe of thyroid glandUBERON:000111996.00gold quality
right adrenal glandUBERON:000123395.94gold quality
corpus epididymisUBERON:000435995.85gold quality
endothelial cellCL:000011595.76gold quality
right adrenal gland cortexUBERON:003582795.73gold quality
renal medullaUBERON:000036295.71gold quality
gall bladderUBERON:000211095.70gold quality
trigeminal ganglionUBERON:000167595.59gold quality
thyroid glandUBERON:000204695.48gold quality
left lobe of thyroid glandUBERON:000112095.47gold quality
left adrenal glandUBERON:000123495.44gold quality
endocervixUBERON:000045895.39gold quality
adrenal cortexUBERON:000123595.39gold quality
descending thoracic aortaUBERON:000234595.39gold quality
left coronary arteryUBERON:000162695.36gold quality
right coronary arteryUBERON:000162595.31gold quality
coronary arteryUBERON:000162195.27gold quality
left adrenal gland cortexUBERON:003582595.27gold quality
thoracic aortaUBERON:000151595.21gold quality
ascending aortaUBERON:000149695.19gold quality
right uterine tubeUBERON:000130295.06gold quality
adrenal glandUBERON:000236995.05gold quality
right ovaryUBERON:000211895.04gold quality
body of uterusUBERON:000985394.94gold quality
aortaUBERON:000094794.91gold quality
ponsUBERON:000098894.91gold quality
C1 segment of cervical spinal cordUBERON:000646994.84gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-GEOD-84465yes2049.60
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 3)

  • CDK4, MDM2, SAS and GLI genes are amplified in leiomyosarcoma, alveolar and embryonal rhabdomyosarcoma (PMID:15024701)
  • TSPAN31 suppresses cell proliferation in human cervical cancer through down-regulation of its antisense pairing with CDK4. (PMID:32207169)
  • Overexpression of Tetraspanin31 contributes to malignant potential and poor outcomes in gastric cancer. (PMID:35307915)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriotspan31ENSDARG00000074554
mus_musculusTspan31ENSMUSG00000006736
rattus_norvegicusTspan31ENSRNOG00000025592

Paralogs (32): TSPAN6 (ENSG00000000003), CD9 (ENSG00000010278), TSPAN9 (ENSG00000011105), TSPAN17 (ENSG00000048140), TSPAN32 (ENSG00000064201), CD82 (ENSG00000085117), TSPAN15 (ENSG00000099282), CD37 (ENSG00000104894), UPK1A (ENSG00000105668), TSPAN12 (ENSG00000106025), TSPAN13 (ENSG00000106537), TSPAN14 (ENSG00000108219), CD81 (ENSG00000110651), TSPAN11 (ENSG00000110900), PRPH2 (ENSG00000112619), UPK1B (ENSG00000114638), TSPAN1 (ENSG00000117472), TSPAN8 (ENSG00000127324), TSPAN16 (ENSG00000130167), TSPAN2 (ENSG00000134198), CD63 (ENSG00000135404), TSPAN3 (ENSG00000140391), CD53 (ENSG00000143119), ROM1 (ENSG00000149489), TSPAN7 (ENSG00000156298), TSPAN18 (ENSG00000157570), TSPAN33 (ENSG00000158457), TSPAN5 (ENSG00000168785), CD151 (ENSG00000177697), TSPAN10 (ENSG00000182612), TSPAN4 (ENSG00000214063), TSPAN19 (ENSG00000231738)

Protein

Protein identifiers

Tetraspanin-31Q12999 (reviewed: Q12999)

Alternative names: Sarcoma-amplified sequence

All UniProt accessions (7): Q12999, F8VNT7, F8VP43, F8VS78, F8VVF8, F8VW54, F8VWE0

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the tetraspanin (TM4SF) family.

RefSeq proteins (3): NP_001317097, NP_001317098, NP_005972* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000301Tetraspanin_animalsFamily
IPR018499Tetraspanin/PeripherinFamily

Pfam: PF00335

UniProt features (14 total): topological domain 5, glycosylation site 4, transmembrane region 4, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q12999-F189.290.64

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Glycosylation sites (4): 100, 109, 117, 134

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 168 (showing top): GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_UP, GSE45365_HEALTHY_VS_MCMV_INFECTION_CD8_TCELL_IFNAR_KO_UP, STARK_PREFRONTAL_CORTEX_22Q11_DELETION_DN, BROWNE_HCMV_INFECTION_48HR_DN, ONKEN_UVEAL_MELANOMA_UP, KESHELAVA_MULTIPLE_DRUG_RESISTANCE, BLALOCK_ALZHEIMERS_DISEASE_UP, NIKOLSKY_BREAST_CANCER_12Q13_Q21_AMPLICON, TSENG_IRS1_TARGETS_DN, DOUGLAS_BMI1_TARGETS_DN, HOOI_ST7_TARGETS_DN, NRF2_01, SPIELMAN_LYMPHOBLAST_EUROPEAN_VS_ASIAN_DN, CETS1P54_01, YIH_RESPONSE_TO_ARSENITE_C3

GO Biological Process (1): positive regulation of cell population proliferation (GO:0008284)

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cell population proliferation1
regulation of cell population proliferation1
positive regulation of cellular process1
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

522 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TSPAN31CD53P19397694
TSPAN31CD37P11049688
TSPAN31TSPAN17Q96FV3666
TSPAN31TM4SF1P30408632
TSPAN31METTL1Q9UBP6595
TSPAN31CD63P08962588
TSPAN31TSPAN5P62079567
TSPAN31CD9P21926562
TSPAN31CD81P18582556
TSPAN31UPK1AO00322555
TSPAN31OS9Q13438545
TSPAN31FRS2Q8WU20531
TSPAN31TSPAN1O60635506
TSPAN31TSPAN8P19075504
TSPAN31CDK4P11802500

IntAct

20 interactions, top by confidence:

ABTypeScore
SLC30A2TSPAN31psi-mi:“MI:0915”(physical association)0.560
CYP4F2TSPAN31psi-mi:“MI:0915”(physical association)0.560
CMTM5TSPAN31psi-mi:“MI:0915”(physical association)0.560
TSPAN31SLC30A2psi-mi:“MI:0915”(physical association)0.560
TSPAN31NAT8psi-mi:“MI:0915”(physical association)0.560
TSPAN2TSPAN31psi-mi:“MI:0915”(physical association)0.560
TSPAN31CMTM5psi-mi:“MI:0915”(physical association)0.560
BMP10TSPAN31psi-mi:“MI:0915”(physical association)0.560
TSPAN31TMEM120Bpsi-mi:“MI:0914”(association)0.350
NAT8TSPAN31psi-mi:“MI:0915”(physical association)0.000
TSPAN2TSPAN31psi-mi:“MI:0915”(physical association)0.000
BMP10TSPAN31psi-mi:“MI:0915”(physical association)0.000

BioGRID (51): TSPAN31 (Two-hybrid), NAT8 (Two-hybrid), BMP10 (Two-hybrid), CMTM5 (Two-hybrid), TSPAN31 (Affinity Capture-RNA), XPO5 (Affinity Capture-MS), ALG3 (Affinity Capture-MS), NRM (Affinity Capture-MS), RHOBTB3 (Affinity Capture-MS), POMK (Affinity Capture-MS), CD81 (Affinity Capture-MS), MFSD1 (Affinity Capture-MS), ATP8 (Affinity Capture-MS), MFSD12 (Affinity Capture-MS), CD63 (Affinity Capture-MS)

ESM2 similar proteins: A0A8M2B5N2, A0A8V0ZLT4, A1L157, B5X3I6, F7BWT7, O15551, O19005, O35566, O95858, P11049, P31053, P35349, P40239, P40240, P40241, P48509, P61170, P61171, Q0VC33, Q12999, Q1JQA4, Q2KHY8, Q32KP1, Q3ZBH3, Q568Y5, Q5BJS2, Q5NCH9, Q5PRC1, Q5RAP8, Q5RH71, Q5U1V9, Q61470, Q63400, Q6GMK6, Q6GQF5, Q765N9, Q7ZUB3, Q80WR1, Q863I4, Q8BM86

Diamond homologs: O95857, Q12999, Q29257, Q32KP1, Q3ZBV0, Q5FVL6, Q5RAP8, Q5U1V9, Q5XHG6, Q7ZUB3, Q7ZWW7, Q9CQ88, Q9D8C2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

178 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance89
Likely benign24
Benign13

Top pathogenic / likely-pathogenic (0)

SpliceAI

1475 predictions. Top by Δscore:

VariantEffectΔscore
12:57741909:TA:Tdonor_loss1.0000
12:57745743:AGCT:Aacceptor_gain1.0000
12:57745744:GCTG:Gacceptor_gain1.0000
12:57745838:G:GTdonor_gain1.0000
12:57745925:G:GTdonor_gain1.0000
12:57746587:A:AGacceptor_gain1.0000
12:57746588:G:GGacceptor_gain1.0000
12:57746588:GAC:Gacceptor_gain1.0000
12:57746588:GACA:Gacceptor_gain1.0000
12:57746650:G:GTdonor_gain1.0000
12:57746718:GCA:Gdonor_gain1.0000
12:57746721:G:GGdonor_gain1.0000
12:57747016:A:AGacceptor_gain1.0000
12:57747017:G:GGacceptor_gain1.0000
12:57749155:C:Adonor_gain1.0000
12:57749452:A:ACdonor_gain1.0000
12:57749453:C:CCdonor_gain1.0000
12:57749453:CT:Cdonor_gain1.0000
12:57741910:A:ACdonor_gain0.9900
12:57741911:C:CCdonor_gain0.9900
12:57741911:CCT:Cdonor_gain0.9900
12:57745743:A:AGacceptor_gain0.9900
12:57745744:G:GGacceptor_gain0.9900
12:57745838:G:Tdonor_gain0.9900
12:57745931:A:AGdonor_gain0.9900
12:57746174:A:AGacceptor_gain0.9900
12:57746175:G:GGacceptor_gain0.9900
12:57746583:TTTCA:Tacceptor_loss0.9900
12:57746584:TTCA:Tacceptor_loss0.9900
12:57746585:TCA:Tacceptor_loss0.9900

AlphaMissense

1383 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
12:57747120:A:CS183R0.996
12:57747122:C:AS183R0.996
12:57747122:C:GS183R0.996
12:57745170:T:CF6L0.987
12:57745172:T:AF6L0.987
12:57745172:T:GF6L0.987
12:57747282:T:CF209L0.987
12:57747284:T:AF209L0.987
12:57747284:T:GF209L0.987
12:57745205:C:AN17K0.984
12:57745205:C:GN17K0.984
12:57745751:A:CS24R0.981
12:57745753:C:AS24R0.981
12:57745753:C:GS24R0.981
12:57747247:G:CR197P0.981
12:57747243:T:CF196L0.980
12:57747245:T:AF196L0.980
12:57747245:T:GF196L0.980
12:57746612:G:CW112C0.965
12:57746612:G:TW112C0.965
12:57747121:G:AS183N0.963
12:57747112:T:CL180P0.962
12:57747117:T:CF182L0.962
12:57747119:T:AF182L0.962
12:57747119:T:GF182L0.962
12:57747222:G:CG189R0.962
12:57745192:T:CL13P0.961
12:57745192:T:AL13H0.957
12:57747051:T:AC160S0.957
12:57747052:G:CC160S0.957

dbSNP variants (sampled 300 via entrez): RS1000416664 (12:57747962 G>A,C), RS1000870693 (12:57748322 C>G), RS1001155355 (12:57749593 T>C), RS1001436631 (12:57745546 C>A,T), RS1002207037 (12:57749098 C>A,T), RS1002653772 (12:57745505 T>C), RS1002924139 (12:57746101 C>G,T), RS1003208178 (12:57747486 G>A), RS1004516189 (12:57745587 C>T), RS1004656804 (12:57750297 G>A,T), RS1004724115 (12:57748846 C>T), RS1005006906 (12:57749964 T>C), RS1005319530 (12:57746941 T>C), RS1005616471 (12:57747406 A>G), RS1006511986 (12:57744719 A>C)

Disease associations

OMIM: gene MIM:181035 | disease phenotypes: MIM:609048, MIM:612219, MIM:167000

GenCC curated gene-disease

Mondo (5): hereditary neoplastic syndrome (MONDO:0015356), familial melanoma (MONDO:0018961), melanoma, cutaneous malignant, susceptibility to, 3 (MONDO:0012183), Ewing sarcoma (MONDO:0012817), ovarian cancer (MONDO:0008170)

Orphanet (5): Inherited cancer-predisposing syndrome (Orphanet:140162), Familial melanoma (Orphanet:618), OBSOLETE: Neuroepithelioma (Orphanet:2677), Skeletal Ewing sarcoma (Orphanet:319), Rare ovarian cancer (Orphanet:213500)

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

MeSH disease descriptors (3)

DescriptorNameTree numbers
D009386Neoplastic Syndromes, HereditaryC04.700; C16.320.700
D010051Ovarian NeoplasmsC04.588.322.455; C12.050.351.500.056.630.705; C12.050.351.937.418.685; C12.100.250.056.630.705; C12.900.418.685; C19.344.410; C19.391.630.705
D012512Sarcoma, EwingC04.557.450.565.575.650.800; C04.557.450.795.620.800

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

PharmGKB variants

1 variants.

VariantGenesLevelScore#Clin annotsDrugs
rs2069502AGAP2, CDK4, MARCHF9, TSPAN3132.001somatropin recombinant

CTD chemical–gene interactions

40 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, increases abundance, increases expression4
cobaltous chloridedecreases expression2
Cadmiumincreases abundance, increases expression, decreases expression2
Valproic Acidincreases expression2
aristolochic acid Idecreases expression1
GSK-J4decreases expression1
bisphenol Aaffects cotreatment, increases expression1
4-hydroxy-2-nonenaldecreases expression1
2,3-bis(3’-hydroxybenzyl)butyrolactoneaffects cotreatment, decreases expression1
4-aminophenylarsenoxideaffects binding, decreases reaction1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
monomethylarsonous aciddecreases expression1
ICG 001increases expression1
abrineincreases expression1
NSC 689534increases expression, affects binding1
(+)-JQ1 compoundincreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acidincreases expression1
Resveratrolaffects cotreatment, decreases expression1
Decitabineaffects expression1
Arsenic Trioxideaffects binding, decreases reaction1
Vorinostatincreases expression1
Acetaminophenincreases expression1
Air Pollutantsdecreases expression, increases abundance1
Arsenicdecreases expression, increases abundance1
Calcitriolincreases expression, affects cotreatment1
Cisplatinaffects expression1
Copperaffects binding, increases expression1
Coumestrolaffects cotreatment, decreases expression1
Dexamethasoneincreases expression, affects cotreatment1

Clinical trials (associated diseases)

270 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT04854018PHASE4COMPLETEDIndo-cyanine Green (ICG) in Paediatric Oncology MIS
NCT00190697PHASE4COMPLETEDA Study of LY353381 (Arzoxifene) for Patients Who Benefitted From This Drug in Other Oncology Trials and Wished to Continue Treatment
NCT00277160PHASE4COMPLETEDA Study of Primary Prophylaxis With Neulasta (Pegfilgrastim) Versus Secondary Prophylaxis After Chemotherapy in Elderly Subjects (>/= 65 Years Old) With Cancer
NCT00727961PHASE4COMPLETEDA Study to Evaluate Efficacy and Tolerance of Caelyx in Patients With Epithelial Ovarian Cancer. (Study P04072)(COMPLETED)
NCT00740116PHASE4COMPLETEDTranexamic Acid in Surgery of Advanced Ovarian Cancer
NCT00817479PHASE4COMPLETEDTumor Gene Expression in Women With Ovarian Cancer
NCT01432015PHASE4COMPLETEDFosaprepitant Versus Aprepitant in the Prevention of Chemotherapy Induced Nausea and Vomiting
NCT01706120PHASE4UNKNOWNStudy of Clinical and Biological Prognostic Factors in Patients With Ovarian Cancer Receiving Carboplatin +Paclitaxel With Bevacizumab
NCT01932125PHASE4COMPLETEDAn Interventional Study of Avastin (Bevacizumab) in Patients With Advanced/Metastatic Epithelial Ovarian Cancer, Fallopian Tube Cancer or Primary Peritoneal Cancer
NCT01953107PHASE4COMPLETEDOral Iron vs. Placebo in Newly Diagnosed Gynecologic Oncology Patients Who Are Surgical Candidates.
NCT02035345PHASE4TERMINATEDSlowed Carboplatin Infusion for Ovarian Cancer Patients Receiving Carboplatin Re-Treatment
NCT02243059PHASE4WITHDRAWNMagnetic Resonance Imaging for Lymph Node Staging in Ovarian Cancer
NCT03164980PHASE4TERMINATEDQoL-Comparison Between Trabectedin/PLD and Pt-based Therapy in Patients With Pt-sensitive Recurrent Ovarian Cancer
NCT03384511PHASE4COMPLETEDThe Use of 18F-ALF-NOTA-PRGD2 PET/CT Scan to Predict the Efficacy and Adverse Events of Apatinib in Malignancies.
NCT03543462PHASE4COMPLETEDDiaphragmatic Resection And Gynecological Ovarian Neoplasm
NCT03752216PHASE4COMPLETEDNIraparib and Quality of LifE is a Longitudinal Study Evaluating in Real Life the Tolerability of Niraparib.
NCT03858166PHASE4TERMINATEDEfficacy and Safety of PEG-rhG-CSF Secondary Prophylaxis vs. Therapeutic Administration in Patients With Ovarian Cancer
NCT04024254PHASE4COMPLETEDA Study of Serum Folate Levels in Patients Treated With Olaparib
NCT04330040PHASE4COMPLETEDProspective Multicentre Phase-IV Clinical Trial of Olaparib in Indian Patients With Ovarian and Metastatic Breast Cancer
NCT04352439PHASE4COMPLETEDAspirin for Prevention of Venous Thromboembolism Among Ovarian Cancer Patients Receiving Neoadjuvant Chemotherapy
NCT05187208PHASE4UNKNOWNPARP Inhibitor Oral Maintenance in Low-Risk Ovarian Cancer
NCT05606692PHASE4RECRUITINGInfluences of Propofol and Sevoflurane Anesthesia in Ovarian Cancer (Anesthetics)
NCT05926336PHASE4RECRUITINGThe Effects of Using Different Anesthetics on the Prognosis of Primary Tumors and Its Mechanism of Action
NCT06412120PHASE4RECRUITINGStudy Evaluating Safety, Tolerability, and Metabolism of Niraparib
NCT06871787PHASE4NOT_YET_RECRUITINGNear-Infrared Fluorescence Imaging With Indocyanine Green to Evaluate Bowel Anastomoses in Gynecologic Oncology Surgery
NCT06887933PHASE4NOT_YET_RECRUITINGA Trial to Evaluate the Safety of Niraparib Tablets in Adult Female Participants With Advanced or Relapsed Epithelial Ovarian Cancer
NCT07469202PHASE4NOT_YET_RECRUITINGCYTALUX Dose Extension Study
NCT00987636PHASE3COMPLETEDStudy in Localized and Disseminated Ewing Sarcoma
NCT01734863PHASE3WITHDRAWNPost-operative Radiotherapy in Poor Responders Ewing’s Sarcoma Patients
NCT02063022PHASE3COMPLETEDEfficacy of Dose Intensification in Patients With Non-metastatic Ewing Sarcoma
NCT02306161PHASE3ACTIVE_NOT_RECRUITINGCombination Chemotherapy With or Without Ganitumab in Treating Patients With Newly Diagnosed Metastatic Ewing Sarcoma
NCT03495921PHASE3TERMINATEDA Trial For Participants With Ewing’s Sarcoma Treated With Vigil in Combination With Irinotecan and Temozolomide
NCT05328258PHASE3RECRUITINGUse of GnRHa During Chemotherapy for Fertility Protection
NCT00001806PHASE3COMPLETEDMethods in Education for Breast Cancer Genetics
NCT00002477PHASE3UNKNOWNAdjuvant Chemotherapy Compared With Observation in Treating Patients With Resected Early Stage Ovarian Epithelial Cancer
NCT00002568PHASE3COMPLETEDCombination Chemotherapy With or Without Surgery in Treating Patients With Stage III Ovarian Epithelial Cancer
NCT00002641PHASE3COMPLETEDSurgery With or Without Chemotherapy in Treating Patients With Soft Tissue Sarcoma
NCT00002717PHASE3COMPLETEDPaclitaxel and Cisplatin in Treating Patients With Stage III or Stage IV Ovarian Cancer or Primary Peritoneal Cancer
NCT00002764PHASE3COMPLETEDSurgery With or Without Combination Chemotherapy in Treating Patients With Lung Metastases From Soft Tissue Sarcoma
NCT00002819PHASE3TERMINATEDChemotherapy With or Without Peripheral Stem Cell Transplantation in Treating Patients With Persistent Ovarian Epithelial Cancer