Target intelligence / Profile preview

HL-60 Human Promyelocytic Leukemia Cell Line (HL-60)

Target
HL-60
Molecular classification
Other
01

Overview

HL-60 is a human promyelocytic leukemia cell line established from the peripheral blood of a 36-year-old woman diagnosed with acute myeloid leukemia. HL-60 cells display a neutrophilic promyelocyte morphology, proliferate in suspension, and can be induced to undergo differentiation into multiple myeloid lineages (granulocytes, monocytes, macrophages) using various agents such as dimethyl sulfoxide, retinoic acid, phorbol esters, or vitamin D3[1][3][4][5][7][8]. The cell line is characterized by genetic instability, amplification of the c-myc oncogene, absence of functional p53, and responsiveness to both physiologic and pharmacologic differentiation stimuli[5][4]. HL-60 cells are extensively used as a model for leukemia research, especially for investigating the molecular pathways of myeloid differentiation, drug screening, toxicity assessment, chromatin and transcriptional changes, and signaling mechanisms relevant to both normal and malignant hematopoiesis[1][4][7]. Unlike a molecular target (such as a receptor or enzyme), HL-60 serves as an experimental system rather than a direct therapeutic target, and thus should not be treated as a druggable molecule itself[1][3][4][7][8].

Other names
HL60HL-60Human Leukemia 60HL-60 cell lineHL60 cell line
02

Mechanism of action

Induction of differentiation, Apoptosis, Modulation of signaling pathways, Cytotoxicity (not direct targeting of 'HL60')

03

Biological functions

Cell proliferationDifferentiationApoptosisModel system for studying leukemiaSignal transduction (via endogenous receptors)
04

Disease associations

CancerAcute myeloid leukemia researchOther (modeling hemopoiesis, differentiation disorders)
05

Safety considerations

Not applicable to therapeutic targetingcell line variabilitygenetic driftdifferences from primary human leukemiapossible misinterpretation if treated as a drug target
06

Interacting drugs

Dimethyl sulfoxide

5 more in the full profile.

07

Biomarkers

c-myc amplificationlack of p53 expressionchanges in nuclear protein phosphorylationmyeloid antigen expression; biomarkers are context-dependent and usually used for experimental readouts rather than patient selection

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