Evidence map›Paper›PMID 25628923›Full record

ArticleAmerican journal of cancer research2015

Myeloid cell leukemia-1 is associated with tumor progression by inhibiting apoptosis and enhancing angiogenesis in colorectal cancer.

Wan-Sik Lee, Young-Lan Park, Nuri Kim, Hyung-Hoon Oh, Dong-Jun Son, Mi-Young Kim, Chan-Young Oak, Cho-Yun Chung, Hyung-Chul Park, Jong-Sun Kim and 4 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Targeting MCL-1 in cancer: current status and perspectives.Journal of hematology & oncology · 2021
    Review
  11. Review
  12. Review
  13. Article
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  15. Article
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  18. Molecular cancer therapeutics · 2017
    Article
  19. Article
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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

14 authors at 1 institution in 1 country.

Wan-Sik LeeDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Young-Lan ParkDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Nuri KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Hyung-Hoon OhDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Dong-Jun SonDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Mi-Young KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Chan-Young OakDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Cho-Yun ChungDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Hyung-Chul ParkDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Jong-Sun KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Dae-Seong MyungDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Sung-Bum ChoDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Hyun-Soo KimDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Young-Eun JooDepartment of Internal Medicine, Chonnam National University Medical School Gwangju, Republic of Korea.
Chonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid cell leukemia-1 (Mcl-1) is a highly expressed anti-apoptotic Bcl-2 protein in cancer. Therefore, inhibition of its expression induces apoptosis in cancer cells and enhances sensitivity to cancer treatment. The aims of this study were to evaluate whether Mcl-1 affects the oncogenic behaviors of colorectal cancer cells, and to document the relationship of its expression with various clinicopathological parameters in colorectal cancer. Mcl-1 knockdown induced apoptosis by activating cleaved caspase-3 and -9, and increasing the expression of the pro-apoptotic protein, PUMA. Mcl-1 knockdown induced cell cycle arrest by decreasing cyclin D1, CDK4 and 6, and by increasing p27 expression. Mcl-1 knockdown decreased both endothelial cell invasion and tube formation, and decreased the expression of VEGF. The phosphorylation level of STAT3 was decreased by Mcl-1 knockdown. The mean apoptotic index value of Mcl-1 positive tumors was significantly lower than that of Mcl-1 negative tumors. The mean microvessel density value of Mcl-1 positive tumors was significantly higher than that of negative tumors. Mcl-1 expression was significantly increased in colorectal cancer, also associated with tumor stage, lymph node metastasis, and poor survival. These results indicate Mcl-1 is associated with tumor progression through its inhibition of apoptosis and enhancement of angiogenesis in colorectal cancer.

Indexed as

angiogenesisapoptosiscolorectal neoplasmMyeloid cell leukemia-1prognosis

Identifiers

PMID25628923
PMCPMC4300705
OpenAlexW1533277415

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.