Target intelligence / Profile preview

pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3 (FTSJ3)

Target
FTSJ3
Molecular classification
Enzyme, RNA methyltransferase (specifically 2'-O-methyltransferase), S-adenosylmethionine-dependent methyltransferase superfamily
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Overview

pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3 (FTSJ3) is an S-adenosylmethionine-dependent enzyme responsible for the 2'-O-methylation of ribosomal RNA, which is critical for proper ribosome biogenesis and function[1][3][10]. FTSJ3 has additional biological roles in the context of disease, notably promoting immune evasion in multiple cancers (including hepatocellular carcinoma) and being hijacked by certain viruses (such as HIV) to modify their RNA and escape innate immune detection[2][4][6]. Increased FTSJ3 activity is associated with tumor progression and reduced survival in cancer patients; its inhibition may synergize with immunotherapies targeting immune checkpoints such as PD-1[2]. Targets such as FTSJ3 that modify RNA and thus influence immune recognition represent emerging nodes for intervention in cancer and infectious disease therapy[2][4][6][10].

Other names
FTSJ3SB92SPB1FtsJ homolog 3FtsJ RNA methyltransferase homolog 3Putative rRNA methyltransferase 3SPB1 RNA methyltransferase homologEPCS3pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ32'-O-ribose RNA methyltransferase SPB1 homologFtsJ RNA 2'-O-methyltransferase 3rRNA (uridine-2'-O-)-methyltransferase 3
02

Mechanism of action

Drugs or molecules targeting FTSJ3 may act by inhibiting its 2'-O-methyltransferase activity, thereby enhancing immune detection of dsRNA and promoting type I interferon responses or synergizing with checkpoint blockade therapies

03

Biological functions

rRNA 2'-O-methylationrRNA (uridine/guanine)-methyltransferase activityProcessing of pre-rRNA to 18S rRNA and 40S ribosomal subunit formationRegulation of innate immunity (by evasion of RNA sensing mechanisms)Maturation of ribosomal RNA (5.8S, LSU, SSU rRNA)
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Disease associations

Cancer (tumor progression, especially hepatocellular carcinoma)Viral infection (notably HIV; assists immune evasion)Myasthenic syndrome, congenital, type 8
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Safety considerations

Potential impact on ribosome biogenesis and general RNA metabolism if broadly inhibited (possible toxicity in normal rapidly dividing cells)Effects on immune homeostasis if global type I IFN pathway is upregulated
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Interacting drugs

Immune checkpoint inhibitors (e.g., anti-PD-1 antibody, in the context of combination therapy in HCC)
07

Biomarkers

FTSJ3 expression level (prognostic/theranostic marker in hepatocellular carcinoma for survival and immune evasion, possible marker for immunotherapy stratification)

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