Target intelligence / Profile preview

Adenovirus replication in tumor cells

Molecular classification
Other
01

Overview

"Adenovirus replication in tumor cells" refers to the use of genetically engineered adenoviruses that can selectively replicate within cancer cells by exploiting tumor-specific mutations (such as in p53 or pRB pathways) or using tumor-selective promoters to control essential viral genes. Upon replication, these viruses induce lysis of the cancer cell (oncolysis), propagate to neighboring malignant cells, and may promote antitumor immune responses. The approach is a foundation of oncolytic virotherapy in cancer; however, replication is governed by multiple viral and cellular factors, and is not in itself a single druggable molecular target. Safety, specificity, and the immune response remain central challenges in clinical development. This entry should ideally map to more precise molecular targets such as individual adenoviral proteins (E1A, E1B, ADP) or their interaction partners (p53, pRB) for structured data.

Other names
Oncolytic adenovirus replicationTumor-selective adenovirus replicationReplicating adenoviral therapy in cancerOncolytic virotherapy (adenoviral subtype)
02

Mechanism of action

Selective replication in tumor cells leading to cancer cell lysis (oncolysis); Stimulation of antitumor immune response; Tropism modification for enhanced tumor selectivity; Apoptosis induction via interaction with tumor suppressor pathways (e.g., p53, pRB)

03

Biological functions

Cell deathCell lysisImmune responseViral replicationApoptosisOncolysis
04

Disease associations

CancerInfection
05

Safety considerations

Off-target viral replication and lysis of normal cellsImmune complications (inflammatory response, cytokine storm)Preexisting antiviral immunity limiting effectivenessViral genome integration or recombination risks
06

Interacting drugs

Oncolytic adenoviral vectors (e.g., ONYX-015 [dl1520])

1 more in the full profile.

07

Biomarkers

Disruption/inactivation of p53 pathwayDefective pRB pathwayHigh S-phase fractionTumor-specific promoters or genetic defects exploited by engineered viruses

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