Evidence map›Paper›PMID 28693242›Full record

ArticleOncology letters2017

Bufalin sensitizes human bladder carcinoma cells to TRAIL-mediated apoptosis.

Kyung-Hwa Kang, Min Ho Han, Jin-Woo Jeong, Cheol Park, Sang-Hyup Lee, Hai Woong Lee, Sang Hoon Hong, Yung Hyun Choi, Su Hyun Hong

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  11. Andrographolide Enhances TRAIL-Induced Apoptosis viaInternational journal of biological sciences · 2019
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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

9 authors at 2 institutions in 1 country.

Kyung-Hwa KangDepartment of Physiology, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Min Ho HanNatural Products Research Team, National Marine Biodiversity Institute of Korea, Seocheon, South Chungcheong 325-902, Republic of Korea.
Jin-Woo JeongDepartment of Biochemistry, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Cheol ParkDepartment of Molecular Biology, College of Natural Science and Human Ecology, Dongeui University, Busan 614-714, Republic of Korea.
Sang-Hyup LeeDepartment of Korean Medical Classics, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Hai Woong LeeDepartment of Public Health, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Sang Hoon HongDepartment of Internal Medicine, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Yung Hyun ChoiDepartment of Biochemistry, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Su Hyun HongDepartment of Biochemistry, Dongeui University College of Korean Medicine, Busan 614-052, Republic of Korea.
Dong-Eui University · KRMarine Biodiversity Institute of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF superfamily, has garnered interest as it is relatively non-toxic to normal cells, but selectively induces apoptotic cell death in multiple types of transformed or malignant cells. Bufalin is the major digoxin-like immunoreactive component of Sum Su, which is obtained from the skin and parotid venom gland of the toad. Bufalin is known to inhibit cell proliferation and induce apoptosis in a variety of cancer cells. The present study investigated whether bufalin promoted TRAIL-induced apoptotic cell death. In the present study, a combined treatment using bufalin and TRAIL significantly increased TRAIL-mediated inhibition of cell viability and increased apoptosis in T24 human bladder cancer cells. The apoptotic effects were associated with the upregulation of death receptor proteins and the downregulation of cellular Fas-associated death domain-like interleukin-1β-converting enzyme inhibitory protein and X-linked inhibitor of apoptosis protein. Furthermore, the data revealed that bufalin and TRAIL activated caspase-3, -8 and -9 and subsequently increased the degradation of poly (ADP-ribose) polymerase. Taken altogether, the nontoxic doses of bufalin and TRAIL sensitized T24 cells to TRAIL-mediated apoptosis. Therefore, bufalin may provide an effective therapeutic strategy for the safe treatment of human bladder cancers that are resistant to TRAIL.

Indexed as

apoptosisbladder cancerbufalincaspasetumor necrosis factor-related apoptosis-inducing ligand

Identifiers

PMID28693242
PMCPMC5494769
OpenAlexW2617532678

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.