Evidence map›Paper›PMID 26909111›Full record

ArticleTheranostics2016

Image-aided Suicide Gene Therapy Utilizing Multifunctional hTERT-targeting Adenovirus for Clinical Translation in Hepatocellular Carcinoma.

Yun-Hee Kim, Kyung Tae Kim, Sang-Jin Lee, Seung-Hee Hong, Ju Young Moon, Eun Kyung Yoon, Sukyoung Kim, Eun Ok Kim, Se Hun Kang, Seok Ki Kim and 7 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.0field-weighted citation impact, top 4% of its field
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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Repair of MutatedCancers · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Drug delivery strategy in hepatocellular carcinoma therapy.Cell communication and signaling : CCS · 2022
    Review
  7. Non-Canonical Splicing and Its Implications in Brain Physiology and Cancer.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Therapeutic applications of trans-splicing.British medical bulletin · 2020
    Article
  11. Article
  12. Review
  13. Stem Cell Therapy for Hepatocellular Carcinoma: Future Perspectives.Advances in experimental medicine and biology · 2020
    Review
  14. Review
  15. Article
  16. Review
  17. RNA Trans-Splicing Modulation via Antisense Molecule Interference.International journal of molecular sciences · 2018
    Article
  18. Article
  19. Article
  20. 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

17 authors at 4 institutions in 2 countries.

Yun-Hee Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea; 2. Graduate School of Cancer Science & Policy, National Cancer Center, Goyang 410-769, Republic of Korea.
Kyung Tae Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Sang-Jin Lee1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea; 2. Graduate School of Cancer Science & Policy, National Cancer Center, Goyang 410-769, Republic of Korea.
Seung-Hee Hong3. Division of Food Science and Culinary Arts, Food and Nutrition Major, Shinhan University, Uijeonbu 480-857, Republic of Korea.
Ju Young Moon1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Eun Kyung Yoon1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea; 4. Department of Life Science, Ewha Womans University, Seoul 120-750, Republic of Korea.
Sukyoung Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Eun Ok Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Se Hun Kang1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Seok Ki Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Sun Il Choi1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea; 4. Department of Life Science, Ewha Womans University, Seoul 120-750, Republic of Korea.
Sung Ho Goh1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Daehong Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea.
Seong-Wook Lee5. Department of Molecular Biology, Institute of Nanosensor and Biotechnology, Dankook University, Youngin 448-701, Republic of Korea.
Mi Ha Ju6. Department of Pathology, Dong-A University College of Medicine, Busan 602-714, Republic of Korea.
Jin Sook Jeong6. Department of Pathology, Dong-A University College of Medicine, Busan 602-714, Republic of Korea.
In-Hoo Kim1. Research Institute and hospital, National Cancer Center, Goyang 410-769, Republic of Korea; 2. Graduate School of Cancer Science & Policy, National Cancer Center, Goyang 410-769, Republic of Korea.
National Cancer Center · USDong-A University · KREwha Womans University · KRShinhan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trans-splicing ribozyme enables to sense and reprogram target RNA into therapeutic transgene and thereby becomes a good sensing device for detection of cancer cells, judging from transgene expression. Previously we proposed PEPCK-Rz-HSVtk (PRT), hTERT targeting trans-splicing ribozyme (Rz) driven by liver-specific promoter phosphoenolpyruvate carboxykinase (PEPCK) with downstream suicide gene, herpes simplex virus thymidine kinase (HSVtk) for hepatocellular carcinoma (HCC) gene therapy. Here, we describe success of a re-engineered adenoviral vector harboring PRT in obtaining greater antitumor activity with less off-target effect for clinical application as a theranostics. We introduced liver-selective apolipoprotein E (ApoE) enhancer to the distal region of PRT unit to augment activity and liver selectivity of PEPCK promoter, and achieved better transduction into liver cancer cells by replacement of serotype 35 fiber knob on additional E4orf1-4 deletion of E1&E3-deleted serotype 5 back bone. We demonstrated that our refined adenovirus harboring PEPCK/ApoE-Rz-HSVtk (Ad-PRT-E) achieved great anti-tumor efficacy and improved ability to specifically target HCC without damaging normal hepatocytes. We also showed noninvasive imaging modalities were successfully employed to monitor both how well a therapeutic gene (HSVtk) was expressed inside tumor and how effectively a gene therapy took an action in terms of tumor growth. Collectively, this study suggests that the advanced therapeutic adenoviruses Ad-PRT-E and its image-aided evaluation system may lead to the powerful strategy for successful clinical translation and the development of clinical protocols for HCC therapy.

Indexed as

Genetic VectorsTransduction, GeneticAdenoviridaeAnimalsCarcinoma, HepatocellularDiagnostic ImagingDisease Models, AnimalGenetic TherapyMice, Inbred BALB CTreatment Outcomecancer gene therapyhepatocellular carcinomain vivo imagingtrans-splicing ribozyme

Identifiers

PMID26909111
PMCPMC4737723
OpenAlexW2292767475

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.