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Prominent proteins in cancer
This is the list of significantly mutated genes (SMGs) and other proteins significantly involved in edgetic perturbations in LUAD.
Perturbation typeGeneCitationCancer typeGene-disease relation
Top gainsSPECC1(Isoform switch)18486272LUADDifferentially expressed in patients with lung adenocarcinoma compared to patient group lung squamous cell carcinoma
Top lossesSUPT3H (Isoform switch)18486272LUADDifferentially expressed in patients with lung adenocarcinoma compared to patient group lung squamous cell carcinoma
Top lossesSUPT3H (Isoform switch)18486272LUADDifferentially expressed in patients with lung adenocarcinoma compared to patient group lung squamous cell carcinoma
Top lossesUSP22 (Isoform switch)18486272LUADDifferentially expressed in patients with lung adenocarcinoma compared to patient group lung squamous cell carcinoma
Top gainsABCC228442702NSCLCABCC2 rs717620 can be used to predict the outcomes of Uygur patients with advanced NSCLC .
Top gainsAGMATUHOD 26(2):103-108 (ww.uhod.org)LUADIncreased level agmatinase in lung cancer patients comapred to heathy controls.
Top gainsCDC25C28566436NSCLCOverexpression of either CDC25C lead to bypass of G2-M arrest and induced ganetespib resistance in vitro and in vivo in KRAS-mutant NSCLC.
Top gainsHPDL23714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top gainsKCNJ1028219421LUADDifferentially expressed in side-population (SP) cells compared to non-SP celles in lung cancer cell line NCI-H460.
Top gainsNEIL327042257LUADDifferentially expressed in lung cancer cells compared to non-cancerous lung tissue sapmles.
Top gainsRGS1719244110LUADIncreased expression in lung cancer samples versus normal control tissue.
Top gainsSGO127526110LUADRAG1−/− Sgo1−/+ mice showed high incidence of lung adenocarcinoma.
Top gainsSOX3030514297LUADSOX30 is a key regulator of desmosomal gene suppressing tumor growth and metastasis in lung adenocarcinoma.
Top gainsSPC2429029446LUADA potential prognostic biomarker SPC24 promotes tumorigenesis and metastasis in lung cancer.
Top cancer-specific gainsSLC25A2121151896LUADSLC25A21 lays in a region of genomic aberrations in lung adenocarcinoma in never smokers.
Top lossesADRA1D26735301SCLCADRA1D potentially has anti-SCLC activity and was administered to a 20 patients with stage 4 SCLC. ADRA1 administration did not result in a statistically significant OS benefit
Top lossesAPOA127648369LUADAPOA1 levels were significantly lower in lung cancer patients.
Top lossesAPP29387243LUADmiR-373-3p promotes lung adenocarcinoma cell proliferation via APP.
Top lossesASB1423714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesASB16Greer RM Dissertation Dallas 2011NSCLCThe expression level of ASB16 was downregulated after treatment by gemcitabine+cisplatin in Non-small-cell lung carcinoma (NSCLC) cells.
Top lossesAVPR211429190NSCLC:SCLCOverxpressed in NSCLC and SCLC.
Top lossesBEX124970476NSCLC:SCLCBEX1 was highly expressed in some NSCLC cell lines and most SCLC cell lines.
Top lossesBMX29208667SCLCEtk (BMX) interacts with PFKFB4 to promote SCLC chemoresistance through regulation of autophagy.
Top lossesBTNL824735754LUAD invasiveDown-regulated in invasive lung adenocarcinoma cells.
Top lossesCAV323714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesCCDC3623714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesCOLEC1023714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesDNASE2BInt J Clin Exp Med 2018;11(11):11846NSCLCDNASE2B serves an important role in the growth of lung cancer cells; and may be considered as a potential biomarker and therapeutic target for lung cancer.
Top lossesENPP623714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesGATA128566697LUADDown-regulated GATA-1 up-regulates interferon regulatory factor 3 in lung adenocarcinoma.
Top lossesGNMT23714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesHSPB323714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesIL9R23065014LUADBoth IL-9 and IL-17 substantially promoted the proliferation and migratory activity of lung cancer cells.
Top lossesINCA125938545:21750715LUADING5 overexpression in lung cancer A549 cells inhibited cell proliferation and invasiveness; while ING5 knockdown in lung cancer H1299 cells promoted cell aggressiveness. The inhibitor of growth protein 5 (ING5) depends on INCA1 as a co-factor for its antiproliferative effects
Top lossesL1TD128093071LUADL1TD1 is tumor-specifically methylated in NSCLCs and that DNA methylation is involved in the transcriptional regulation of these genes.
Top lossesMYOC23714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesOLIG117388669NSCLCOLIG1 protein expression significantly correlates with overall survival in NSCLC patients.
Top lossesPPARGC1B22777349NSCLCPGC-1beta mediates adaptive chemoresistance to cisplatin associated with mitochondrial DNA mutations in non-small-cell lung cancer cells
Top lossesPTPN523714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesRAB40A23714854SCLCDifferentially expressed in SCLC tumor samples compared to normal samples.
Top lossesSH3GL222968441NSCLCSH3GL2 is frequently deleted in NSCLC and downregulates tumor growth by modulating EGFR signaling.
Top lossesSH3GL315087295LUADDifferentially expressed in lung cancer samples.
Top lossesSLC2A4Wei C; AACR Annual Meeting 2017; Washington DCLUADGLUT4 (SLC2A4) exhibits a non-canonical role of regulating lung cancer metastasis.
Top lossesTCAP25485619SCLCDifferentially expressed in SCLC cell lines (high-throughput experiments).
Top lossesWNT3A29218239NSCLCWnt3a expression is positively correlated with the of NSCLC patients.
Top cancer-specific lossesPPARGC1B22777349NSCLCPGC-1beta mediates adaptive chemoresistance to cisplatin associated with mitochondrial DNA mutations in NSCLC.
SMGs within edgetic gains or lossesAKT130556874LUADLINC00324 exerts tumor-promoting functions in lung adenocarcinoma via targeting miR-615-5p/AKT1 axis
SMGs within edgetic gains or lossesARID1A24566899NSCLCARID1A is downregulated in NSCLC and regulates cell proliferation and apoptosis.
SMGs within edgetic gains or lossesBAP121941004LUADGermline BAP1 mutation predisposes to uveal melanoma; lung adenocarcinoma; meningioma; and other cancers.
SMGs within edgetic gains or lossesCTNNB110070329LUADReduced beta-catenin expression in surgically treated NSCLC is clearly associated with lymph node metastasis and an infavourable prognosis.
SMGs within edgetic gains or lossesCUL321795997NSCLCMultiple component disruption of KEAP1-CUL3-RBX1 complex represents a novel mechanism of NF-κB activation in NSCLC.
SMGs within edgetic gains or lossesDROSHA29236960NSCLCMicroRNA-128-3p-mediated depletion of Drosha promotes lung cancer cell migration.
SMGs within edgetic gains or lossesEGFR28430586NSCLCEGFR has been identified as an oncogenic driver of NSCLC; especially activating mutations EGFR and its inhibition with specific TKIs can generate dramatic tumor responses.
SMGs within edgetic gains or lossesFGFR230013642NSCLCThe expression level of FGFR2 mRNA in the NSCLC tissues was significantly higher than that in the adjacent normal tissues.
SMGs within edgetic gains or lossesKRAS28570035LUADKRAS (V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog) is the most frequently mutated oncogene in lung adenocarcinoma and a member of the RAS family of GTPases; which also includes HRAS and NRAS.
SMGs within edgetic gains or lossesMET28373408NSCLC In NSCLC; aberrant MET signaling can occur through a number of mechanisms that collectively represent a significant proportion of patients. These include MET or HGF protein overexpression; MET gene amplification; MET gene mutation or fusion/rearrangement; or aberrations in downstream signaling or regulatory components
SMGs within edgetic gains or lossesPIK3CA23674897LUADPIK3CA mutations H1047R and H1047L are significant genetic alterations in lung adenocarcinoma.
SMGs within edgetic gains or lossesSMARCA428555282NSCLCSMARCA4-deficient pulmonary adenocarcinoma is emerging as a distinctive; albeit phenotypically heterogeneous molecular subgroup of TTF1-negative NSCLC.
SMGs within edgetic gains or lossesSTK1129764856LUADTP53; STK11; and EGFR mutations predict tumor immune profile and the response to anti-PD-1 in lung adenocarcinoma.
SMGs within edgetic gains or lossesTP5329764856LUADTP53; STK11; and EGFR mutations predict tumor immune profile and the response to anti-PD-1 in lung adenocarcinoma.

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