Evidence map›Paper›PMID 37843231›Full record

ArticleCancer medicine2023

The tumor suppressive effect and apoptotic mechanism of TRAIL gene-containing recombinant NDV in TRAIL-resistant colorectal cancer HT-29 cells and TRAIL-nonresistant HCT116 cells, with each cell bearing a mouse model.

Bo-Kyoung Jung, Yong Hee An, Sung Hoon Jang, Gyoungah Ryu, Saet-Byel Jung, Seonhee Kim, Cuk-Seong Kim, Hyun Jang

Abstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. [Programmed cell death in paramyxovirus infection].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Review
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Bo-Kyoung JungLibentech Co. LTD, Daejeon, Republic of Korea.
Yong Hee AnLibentech Co. LTD, Daejeon, Republic of Korea.
Sung Hoon JangGraduate School of Medical Science, College of medicine, Yonsei University, Seoul, Republic of Korea.
Gyoungah RyuLibentech Co. LTD, Daejeon, Republic of Korea.
Saet-Byel JungLibentech Co. LTD, Daejeon, Republic of Korea.
Seonhee KimDepartment of Physiology & Medical Science, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Cuk-Seong KimDepartment of Physiology & Medical Science, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Hyun JangLibentech Co. LTD, Daejeon, Republic of Korea.ORCID 0000-0002-5267-4360

Funding

Ministry of SMEs and Startups S3271268
6 · The paper itself

Abstract

backgroundTRAIL is an anticancer drug that induces cancer cell apoptosis by interacting with death receptors (DRs). However, owing to low cell-surface expression of DRs, certain colorectal cancer (CRC) cells resist TRAIL-induced apoptosis. Newcastle disease virus (NDV) infection can elevate DR protein expression in cancer cells, potentially influencing their TRAIL sensitivity. However, the precise mechanism by which NDV infection modulates DR expression and impacts TRAIL sensitivity in cancer cells remains unknown.

methodsHerein, we developed nonpathogenic NDV VG/GA strain-based recombinant NDV (rNDV) and TRAIL gene-containing rNDV (rNDV-TRAIL). We observed that viral infections lead to increased DR and TRAIL expressions and activate signaling proteins involved in intrinsic and extrinsic apoptosis pathways. Experiments were conducted in vitro using TRAIL-resistant CRC cells (HT-29) and nonresistant CRC cells (HCT116) and in vivo using relevant mouse models.

resultsrNDV-TRAIL was found to exhibit better apoptotic efficacy than rNDV in CRC cells. Notably, rNDV-TRAIL had the stronger cancer cell-killing effect in TRAIL-resistant CRC cells. Western blot analyses showed that both rNDV and rNDV-TRAIL infections activate signaling proteins involved in the intrinsic and extrinsic apoptotic pathways. Notably, rNDV-TRAIL promotes concurrent intrinsic and extrinsic signal transduction in both HCT-116 and HT-29 cells.

conclusionsTherefore, rNDV-TRAIL infection effectively enhances DR expression in DR-depressed HT-29 cells. Moreover, the TRAIL protein expressed by rNDV-TRAIL effectively interacts with DR, leading to enhanced apoptosis in TRAIL-resistant HT-29 cells. Therefore, rNDV-TRAIL has potential as a promising therapeutic approach for treating TRAIL-resistant cancers.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsAnimalsApoptosisHCT116 CellsHT29 CellsHumansMiceNewcastle disease virusTNF-Related Apoptosis-Inducing LigandAntineoplastic AgentsTNF-Related Apoptosis-Inducing Ligandapoptosiscolorectal cancerviral infectionviral oncology

Identifiers

PMID37843231
PMCPMC10652305

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.