Target intelligence / Profile preview

Doublecortin-like kinase 1 (DCLK1) (DCLK1)

Target
DCLK1
Molecular classification
Serine/threonine-protein kinase, Microtubule-associated protein, Receptor
01

Overview

Doublecortin-like kinase 1 (DCLK1) is a microtubule-associated serine/threonine kinase that serves as a definitive marker for cancer stem cells (CSCs) in various solid tumors, including colorectal and pancreatic cancers (Sureban et al., 2011, PubMed: 21212444). While the long isoform (DCLK1-L) is primarily intracellular and expressed in normal tissues, specific cancer-associated short isoforms (DCLK1-S or ASV) are overexpressed in malignant cells and uniquely exhibit an extracellular domain (ECD) on the cell surface (Weygant et al., 2015, PubMed: 26053294). This tumor-specific surface expression makes the DCLK1-S ECD a highly attractive target for therapeutic interventions such as monoclonal antibodies (e.g., CBT-15) and CAR-T cell therapies, which can selectively eliminate CSCs while sparing normal cells (Westphalen et al., 2014, PubMed: 24441104). DCLK1 signaling is a key driver of the epithelial-mesenchymal transition (EMT) and promotes tumor survival, metastasis, and resistance to chemotherapy (Nakanishi et al., 2013, PubMed: 23292625). Targeting the extracellular domain allows for the delivery of cytotoxic payloads via antibody-drug conjugates (ADCs) or direct immune-mediated destruction of the tumor-initiating cell population.

Other names
DCAMKL1Doublecortin-like and CAM kinase-like 1CLICK-IDCLKDCLK1-SDCLK1-ASVCancer stem cell marker DCLK1
02

Mechanism of action

Antibody-mediated targeting of the extracellular domain of the DCLK1-S isoform to induce cell death or deliver payloads; small molecule inhibition of the intracellular kinase domain to disrupt oncogenic signaling pathways.

03

Biological functions

Signal transductionCell proliferationCell migrationEpithelial-mesenchymal transitionCancer stem cell maintenance
04

Disease associations

Cancer
05

Safety considerations

Potential neurotoxicity due to DCLK1 role in brain developmentPotential damage to normal intestinal tuft cellsRequirement for high isoform specificity to avoid off-tumor effects
06

Interacting drugs

CBT-15

3 more in the full profile.

07

Biomarkers

Cell-surface DCLK1-S expressionCirculating DCLK1 protein levelsDCLK1 mRNA splice variants

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