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GENE:

CD52 (CD52 Molecule)

i
Other names: CD52, CD52 Molecule, HE5, EDDM5, CDW52, Human Epididymis-Specific Protein 5, CD52 Antigen (CAMPATH-1 Antigen), Epididymal Secretory Protein E5, Cambridge Pathology 1 Antigen, CAMPATH-1 Antigen, Epididymis Secretory Sperm Binding Protein Li 171mP, CDW52 Antigen (CAMPATH-1 Antigen), CD52 Antigen, HEL-S-171mP, CDw52, He5
29d
CD52 signaling via macrophage Siglec-G represents a therapeutic target for cancer immunotherapy. (PubMed, NPJ Breast Cancer)
Additionally, cotreatment with anti-CD52 sensitized tumor cells to PD-1 blockade therapy in the spontaneous MMTV-PyMT TNBC model. Our findings identify CD52 as a prominently expressed anti-phagocytic checkpoint in TNBC and reveal the therapeutic potential of dual PD-1/CD52 blockade as a novel immunotherapeutic strategy.
Journal • PD(L)-1 Biomarker • IO biomarker
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CD52 (CD52 Molecule)
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CD52 expression
29d
Single cell transcriptomics derived combinatorial markers distinguished leukemic stem cells from hematopoietic stem cells in acute myeloid leukemia. (PubMed, Leuk Res)
Incorporating these markers in combination with established aberrant markers can enhance the identification of LSCs and help distinguish them from HSCs in both CD34 + and CD34- AML. Our findings support the use of an expanded combinatorial marker panel and warrants its further evaluation in a larger AML cohort, particularly in the context of measurable residual disease (MRD) assessment, prognostication and correlation with treatment response and survival outcomes.
Journal • IO biomarker
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CD38 (CD38 Molecule) • CD34 (CD34 molecule) • CD52 (CD52 Molecule) • CD48 (CD48 Molecule) • CD96 (CD96 Molecule)
1m
CiFGNA: Comprehensive information-based functional gene network analysis. (PubMed, Stat Methods Med Res)
Key findings revealed gene networks centered on CD52, EPCAM, and TNFRSF12A as markers of drug-response phenotypes, suggesting that targeting resistance-related molecular interactions (e.g. CD52 and EPCAM) or enhancing sensitivity-associated markers such as TNFRSF12A may improve chemotherapy efficacy. Overall, CiFGNA offers a powerful, generalizable tool for interpreting complex gene networks and advancing systems-level understanding of disease mechanisms.
Journal
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EPCAM (Epithelial cell adhesion molecule) • CD52 (CD52 Molecule) • TNFRSF12A (TNF Receptor Superfamily Member 12A)
2ms
RVd and CyBorD therapies remodel B-cell maturation signaling and alter immune and clonal architecture in multiple myeloma. (PubMed, Cancer Biol Ther)
Although lenalidomide/bortezomib/dexamethasone (RVd) and cyclophosphamide/bortezomib/dexamethasone (CyBorD) are clinically effective, their precise impacts on PC/B-cell maturation remain unclear. RVd responders further downregulated CD56, CD269, and CD329, and increased CD243. These shared and divergent modulations elucidate the molecular underpinnings of RVd and CyBorD efficacy and inform precision regimen selection.
Journal
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MYC (V-myc avian myelocytomatosis viral oncogene homolog) • FGFR3 (Fibroblast growth factor receptor 3) • NOTCH1 (Notch 1) • MYD88 (MYD88 Innate Immune Signal Transduction Adaptor) • CXCR4 (Chemokine (C-X-C motif) receptor 4) • TNFRSF17 (TNF Receptor Superfamily Member 17) • RARA (Retinoic Acid Receptor Alpha) • ABCG2 (ATP Binding Cassette Subfamily G Member 2) • PAX5 (Paired Box 5) • KLF4 (Kruppel-like factor 4) • NCAM1 (Neural cell adhesion molecule 1) • SDC1 (Syndecan 1) • CD200 (CD200 Molecule) • IRF4 (Interferon regulatory factor 4) • CD52 (CD52 Molecule) • PRDM1 (PR/SET Domain 1) • NANOG (Nanog Homeobox) • NES (Nestin) • XBP1 (X-box-binding protein 1) • CD81 (CD81 Molecule) • NSD2 (Nuclear Receptor Binding SET Domain Protein 2) • SLAMF7 (SLAM Family Member 7) • SIGLEC9 (Sialic Acid Binding Ig Like Lectin 9)
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lenalidomide • bortezomib • cyclophosphamide
3ms
Universal Base-Edited CAR7 T Cells for T-Cell Acute Lymphoblastic Leukemia. (PubMed, N Engl J Med)
Universal BE-CAR7 T cells induced leukemic remission in patients with relapsed or refractory T-cell ALL, thus allowing successful allogeneic hematopoietic stem-cell transplantation in most of the patients. (Funded by the Medical Research Council and others; ISRCTN Registry number, ISRCTN15323014.).
Journal
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CD52 (CD52 Molecule)
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cyclophosphamide • Campath (alemtuzumab) • fludarabine IV • BE CAR7 T
3ms
Integration of Transcriptome Profiling and Single-Cell Sequencing Analysis to Establish a CD8+ T Cell-Related Prognostic Model for Patients With NSCLC: From Assessment to Therapy. (PubMed, Cancer Med)
This study constructed an innovative CD8+ T cell-related risk model, advancing clinical diagnosis and offering valuable therapeutic strategies for patients with NSCLC.
Journal • IO biomarker
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CD8 (cluster of differentiation 8) • CD69 (CD69 Molecule) • CD52 (CD52 Molecule) • PLIN2 (Perilipin)
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paclitaxel
4ms
Elevated NUF2 and CD52 expression predict platinum-based chemoresistance and poor prognosis in non-small cell lung cancer. (PubMed, Discov Oncol)
High expression of NUF2 and CD52 is closely linked to platinum resistance and aggressive tumor behavior in NSCLC, and serves as an independent predictor of adverse outcomes. These markers may hold potential as prognostic indicators and therapeutic targets in chemoresistant NSCLC. These findings, while promising, are based on a single-center retrospective cohort and should be validated in larger, independent studies to confirm their clinical utility.
Journal
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CD52 (CD52 Molecule)
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CD52 expression
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cisplatin • gemcitabine
4ms
Exploring CD19-targeted Immunotherapy Strategies for Human B-cell Lymphoma. (PubMed, Arch Razi Inst)
There are several FDA-approved anti-CD19 CAR-T cells, including Axicabtagene Ciloleucel, Tisagenlecleucel, and Lisocabtagene Maraleucel, as well as anti-CD19 monoclonal antibodies (mABs), such as loncastuximab tesirine and tafasitamab...Blinatumomab, the inaugural FDA-approved antibody to be produced using BiTE technology, has demonstrated notable benefits in clinical trials investigating its use in the treatment of B-cell acute lymphoblastic leukemia (B-ALL)...Furthermore, we engaged in a discourse on the various treatment options concerning CD19 targeting, accompanied by an exposition of the pertinent clinical studies. In this regard, the efficacy, safety, and limitations of each option were thoroughly delineated.
Review • Journal
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CD20 (Membrane Spanning 4-Domains A1) • TNFRSF8 (TNF Receptor Superfamily Member 8) • CD79B (CD79b Molecule) • CD52 (CD52 Molecule)
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Blincyto (blinatumomab) • Yescarta (axicabtagene ciloleucel) • Breyanzi (lisocabtagene maraleucel) • Kymriah (tisagenlecleucel-T) • Zynlonta (loncastuximab tesirine-lpyl) • Monjuvi (tafasitamab-cxix)
4ms
Universal CAR-T Cell Therapy for Cancer Treatment: Advances and Challenges. (PubMed, Oncol Res)
Although trials for solid tumors (e.g., CYAD-101, CTX130) show modest responses, challenges such as tumor heterogeneity and T cell exhaustion remain. Future research should focus on optimizing gene editing precision, integrating combination therapies, and advancing scalable manufacturing platforms. With expanded targets and cell types, UCAR therapies show promise for both hematologic and solid tumors, reshaping cancer treatment and patient outcomes.
Review • Journal
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CD52 (CD52 Molecule)
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CYAD-101 • CTX130
4ms
Neoadjuvant chemotherapy modulates mast cell phenotypes and immune infiltration in high-grade serous carcinoma. (PubMed, Gynecol Oncol)
Successful NACT was associated with a reduction in CD52 + KIT+ mast cells and an increase in the JUN+/TNFRSF12A+ subpopulation. The increased infiltration of KIT-expressing mast cells may serve as a prognostic biomarker for HGSC following NACT and represent a potential novel therapeutic target to enhance NACT efficacy.
Journal
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KIT (KIT proto-oncogene, receptor tyrosine kinase) • CD8 (cluster of differentiation 8) • CD52 (CD52 Molecule) • TNFRSF12A (TNF Receptor Superfamily Member 12A)
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KIT expression
5ms
Genes with altered expression by 5-Aza treatment in myeloid leukemia cells through methylation in intron 1. (PubMed, Leuk Res)
5-Azacitidine (5-Aza) is a hypomethylating agent with demonstrated therapeutic efficacy for myeloid leukemia...The results revealed that two genes (HDC and MICALL2) with increased expression in leukemia cells after 5-Aza treatment were associated with better overall survival, while six genes (BTG2, CD52, PECAM1, PIK3IP1, PTGS2, and TREML2) correlated with worse overall survival. This study revealed that the epigenetic regulation by DNA demethylation in intron 1 has an important role of 5-Aza treatment in myeloid leukemia cells, and suggests novel targets for the development of combination therapy with 5-Aza.
Journal
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PTGS2 (Prostaglandin-Endoperoxide Synthase 2) • CD31 (Platelet and endothelial cell adhesion molecule 1) • CD52 (CD52 Molecule) • PECAM1 (Platelet And Endothelial Cell Adhesion Molecule 1) • BTG2 (BTG Anti-Proliferation Factor 2) • PACERR (PTGS2 Antisense NFKB1 Complex-Mediated Expression Regulator RNA)
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azacitidine
6ms
Regulation of Tetraspanin CD63 in Chronic Myeloid Leukemia (CML): Single-Cell Analysis of Asymmetric Hematopoietic Stem Cell Division Genes. (PubMed, Bioengineering (Basel))
The single-cell trajectory reconstitution analysis in CP samples showed CD63 regulation highlighting a trajectory cluster implicating HSPB1, PIM2, ANXA5, LAMTOR1, CFL1, CD52, RAD52, MEIS1, and PDIA3, known to be implicated in hematopoietic malignancies. (4) Regulation of CD63, a tetraspanin involved in the asymmetric division of hematopoietic stem cells, was found to be associated with poor prognosis during CML progression and could be a potential new therapeutic target.
Journal
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MEIS1 (Meis Homeobox 1) • CD52 (CD52 Molecule) • RAD52 (RAD52 Homolog DNA Repair Protein) • HSPB1 (Heat shock 27kDa protein 1) • PDIA3 (Protein Disulfide Isomerase Family A Member 3) • ANXA5 (Annexin A5) • LAMP2 (Lysosomal Associated Membrane Protein 2)