Evidence map›Paper›PMID 12879013›Full record

ArticleOncogene2003

Identification and differential expression of novel human cervical cancer oncogene HCCR-2 in human cancers and its involvement in p53 stabilization.

Jesang Ko, Young Han Lee, Seung Yong Hwang, Youn Soo Lee, Seung Min Shin, Jae Hoon Hwang, Jin Kim, Yong Wook Kim, Sung-Wuk Jang, Zae Young Ryoo and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

31 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. LETMD1 is required for mitochondrial structure and thermogenic function of brown adipocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. The role of human cervical cancer oncogene in cancer progression.International journal of clinical and experimental medicine · 2015
    Review
  16. Article
  17. Human cervical cancer oncogene-1 over expression in colon cancer and its clinical significance.International journal of clinical and experimental medicine · 2015
    Article
  18. Article
  19. Article
  20. Clinical implication of elevated human cervical cancer oncogene-1 expression in esophageal squamous cell carcinoma.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2012
    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

13 authors at 4 institutions in 1 country.

Jesang KoAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul 138-736, South Korea.
Young Han Lee
Seung Yong Hwang
Youn Soo Lee
Seung Min Shin
Jae Hoon Hwang
Jin Kim
Yong Wook Kim
Sung-Wuk Jang
Zae Young Ryoo
In-Kyung Kim
Sung Eun Namkoong
Jin Woo Kim
Catholic University of Korea · KRHanyang University · KRUlsan College · KRYeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basic studies of oncogenesis have demonstrated that either the elevated production of particular oncogene proteins or the occurrence of qualitative abnormalities in oncogenes can contribute to neoplastic cellular transformation. The purpose of this study was to identify unique oncogenes that are differentially expressed in human cancers and characterize their functions in tumorigenesis. To discover new putative oncogenes, the differential display RT-PCR method was applied using normal cervical tissues, cervical cancer cell lines, cervical cancer tissues, and metastatic tissues. We identified a new human cervical cancer oncogene HCCR-2 that was overexpressed in various human tumors including leukemia, lymphoma, and carcinomas of the breast, kidney, ovary, stomach, colon, and uterine cervix. Ectopic expression of HCCR-2 resulted in direct tumorigenic conversions of NIH/3T3 and Rat1 fibroblasts. Nude mice injected with NIH/3T3 cells stably transfected with HCCR-2 formed tumors in 4 weeks. The resultant tumors display characteristics of an epithelial carcinoma. In HCCR-2 transfected NCI-H460 cells and RKO cells, stabilization of the p53 tumor suppressor occurred without genetic mutation and correlated with functional impairment, as indicated by the defective induction of p53-induced p21(WAF1), MDM2, and bax. These results indicate that HCCR-2 probably represents a new oncogene that is related to tumorigenesis, functioning as a negative regulator of the p53 tumor suppressor.

Indexed as

Phosphotransferases3T3 CellsAmino Acid SequenceAnimalsBacterial Outer Membrane ProteinsBlotting, NorthernBlotting, WesternCell DifferentiationCell LineCell Transformation, NeoplasticCervix UteriFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunohistochemistryBacterial Outer Membrane ProteinsCdk5r1 protein, mouseCdk5r1 protein, ratLETMD1 protein, humanLipoproteinsLuciferasesOncogene ProteinsPhosphotransferasesProto-Oncogene Proteins

Identifiers

PMID12879013
OpenAlexW1967831691

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.