Evidence map›Paper›PMID 30987009›Full record

ArticleNutrients2019

Luteolin Shifts Oxaliplatin-Induced Cell Cycle Arrest at G₀/G₁ to Apoptosis in HCT116 Human Colorectal Carcinoma Cells.

Chan Ho Jang, Nayoung Moon, Jisun Oh, Jong-Sang Kim

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. 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
1.9field-weighted citation impact, top 14% 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, 43 citations in OpenAlex.

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  12. Application of Luteolin in Neoplasms and Nonneoplastic Diseases.International journal of molecular sciences · 2023
    Review
  13. Immunopharmacological Activities of Luteolin in Chronic Diseases.International journal of molecular sciences · 2023
    Review
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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

4 authors at 1 institution in 1 country.

Chan Ho JangSchool of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea. cksghwkd7@gmail.com.
Nayoung MoonSchool of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea. moonna1008@naver.com.
Jisun OhSchool of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea. j.oh@knu.ac.kr.
Jong-Sang KimSchool of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea. vision@knu.ac.kr.ORCID 0000-0003-0483-7230
Kyungpook National University · KR

Funding

National Research Foundation of Korea 2017R1A2B4005087
6 · The paper itself

Abstract

Certain antioxidative flavonoids are known to activate nuclear factor E2-related factor 2 (Nrf2), a transcription factor that regulates cellular antioxidants and detoxifying response and is reportedly highly activated in many types of cancers. Few studies on the potential undesired effects of flavonoid intake during chemotherapy have been conducted, yet Nrf2 activators could favor cancer cell survival by attenuating chemotherapeutic efficiency. This study aimed to examine if luteolin, an Nrf2 activator, hinders chemotherapeutic activity of oxaliplatin, a potent anticancer agent for colorectal cancer, in HCT116 cells. Luteolin treatment strongly increased the transcriptional activity of the antioxidant response element in HCT116 cells and induced the protein expression of heme oxygenase-1, which were indicative of its Nrf2-inducing potential. Intriguingly, 25 μM luteolin reduced cell viability through apoptotic induction, which was intensified in p53-expressing cells while 1 μM oxaliplatin caused cell cycle arrest at G₀/G₁-phase via the p53/p21-dependent mechanism. Moreover, luteolin treatment was found to reduce oxaliplatin-treated p53-null cell viability and colony counts further, thereby demonstrating an additional effect of luteolin in the killing of human colorectal tumor HCT116 cells not expressing functional p53 protein. The findings suggest that luteolin can induce p53-mediated apoptosis regardless of oxaliplatin treatment and may eliminate oxaliplatin-resistant p53-null colorectal cells.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsAntioxidant Response ElementsApoptosisColorectal NeoplasmsCyclin-Dependent Kinase Inhibitor p21G1 Phase Cell Cycle CheckpointsHCT116 CellsHeme Oxygenase-1HumansLuteolinNF-E2-Related Factor 2OxaliplatinResting Phase, Cell CycleSignal TransductionTumor Suppressor Protein p53CDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21Heme Oxygenase-1HMOX1 protein, humanLuteolinNFE2L2 protein, humanNF-E2-Related Factor 2OxaliplatinTP53 protein, humanTumor Suppressor Protein p53anticancercolorectal cancerflavonoidluteolinoxaliplatin

Identifiers

PMID30987009
PMCPMC6521147
OpenAlexW2931298055

What OpenQuestion 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 OpenQuestion graph.