Target intelligence / Profile preview

Chromosome segregation 1 like protein (CSE1L)

Target
CSE1L
Molecular classification
Nuclear transport protein, Exportin, Other
01

Overview

Chromosome segregation 1 like protein (CSE1L, also known as Exportin-2, CAS, or XPO2) is a nuclear transport receptor that mediates the re-export of importin-alpha from the nucleus to the cytoplasm after it has delivered NLS-cargo proteins across the nuclear pore complex. CSE1L plays a vital role in nuclear-cytoplasmic transport by binding importin-alpha in the nucleus and releasing it in the cytoplasm in a process regulated by RanGTP and its co-factors. Beyond its transport function, CSE1L indirectly regulates gene silencing via the nuclear import of chromatin-associated and gene-repressive proteins, and has a noted role in cell proliferation, apoptosis inhibition, and tumorigenesis. Overexpression of CSE1L is often linked with cancer progression, metastasis, and poor patient prognosis. While not yet directly targeted by approved drugs, CSE1L is of significant interest as a potential therapeutic target and biomarker in oncology[1][2][3].

Other names
Exportin-2CASXPO2Importin-alpha re-exporterCellular apoptosis susceptibility proteinChromosome segregation 1-like proteinCSE1Exp2BCR/ABL fusion protein (historical/informal; not commonly used in modern nomenclature)
02

Mechanism of action

Drugs targeting CSE1L (if developed) would likely modulate nuclear export/import of key cargo proteins, impacting signal transduction pathways (e.g., NF-κB/MAPK)[3]. Inhibition could impact tumor cell proliferation and promote apoptosis by trapping nuclear factors or blocking export of growth-promoting proteins[3].

03

Biological functions

Nuclear export of importin-alphaRegulation of nucleocytoplasmic transportCell proliferationApoptosis regulationGene silencing (indirect, through nuclear import of repressors)Chromosome segregation
04

Disease associations

CancerTumor progression and metastasisOther (possible developmental disorders, suggested by rare links to integrative agnosia and sex reversal)
05

Safety considerations

Targeting CSE1L may affect essential nucleocytoplasmic transport in normal cells, leading to possible toxicity[1].Disrupting CSE1L can perturb fundamental cell processes (cell cycle, apoptosis, gene regulation), presenting risks of broad systemic effects if not properly targeted[1][3].
06

Interacting drugs

No clinically approved drugs are currently characterized as direct CSE1L modulators.

1 more in the full profile.

07

Biomarkers

CSE1L overexpression (consistently observed in various cancers, including non-small cell lung cancer) is a potential biomarker for poor prognosis and therapeutic response[3].

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