Evidence map›Paper›PMID 37894822›Full record

ArticleInternational journal of molecular sciences2023

Biological Evaluation of 8-Methoxy-2,5-dimethyl-5H-indolo[2,3-b] Quinoline as a Potential Antitumor Agent via PI3K/AKT/mTOR Signaling.

Yunhao Ma, Hongmei Zhu, Xinrong Jiang, Zhongkun Zhou, Yong Zhou, Yanan Tian, Hao Zhang, Mengze Sun, Lixue Tu, Juan Lu and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

14 authors at 2 institutions in 2 countries.

Yunhao MaSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Hongmei ZhuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Xinrong JiangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Zhongkun ZhouSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Yong ZhouSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Yanan TianFaculty of Applied Science, Macao Polytechnic University, Macao, China.
Hao ZhangSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Mengze SunSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Lixue TuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Juan LuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Yuqing NiuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Huanxiang LiuFaculty of Applied Science, Macao Polytechnic University, Macao, China.ORCID 0000-0002-9284-3667
Yingqian LiuSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.
Peng ChenSchool of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.ORCID 0000-0003-4402-4568
Lanzhou University · CNMacao Polytechnic University · MO

Funding

Innovation and Entrepreneurship Training Program of Lanzhou University, China cxcy2023013Medical Innovation and Development Project of Lanzhou University lzuyxcy-2022-95Technology Program of Lanzhou City 2022-2-52 and 2022-2-67the College Students' Innovation and Entrepreneurship Program of Lanzhou University, China 20230260008the Key Research and Development Program of Gansu Province 21YF5FA112the Technological Innovation Guidance Program of Gansu Province 21CX6QA127
6 · The paper itself

Abstract

Chemotherapy is commonly used clinically to treat colorectal cancer, but it is usually prone to drug resistance, so novel drugs need to be developed continuously to treat colorectal cancer. Neocryptolepine derivatives have attracted a lot of attention because of their good cytotoxic activity; however, cytotoxicity studies on colorectal cancer cells are scarce. In this study, the cytotoxicity of 8-methoxy-2,5-dimethyl-5H-indolo[2,3-b] quinoline (MMNC) in colorectal cells was evaluated. The results showed that MMNC inhibits the proliferation of HCT116 and Caco-2 cells, blocks the cell cycle in the G2/M phase, decreases the cell mitochondrial membrane potential and induces apoptosis. In addition, the results of western blot experiments suggest that MMNC exerts cytotoxicity by inhibiting the expression of PI3K/AKT/mTOR signaling pathway-related proteins. Based on these results, MMNC is a promising lead compound for anticancer activity in the treatment of human colorectal cancer.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsQuinolinesApoptosisCaco-2 CellsCell Line, TumorCell ProliferationHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuinolinesTOR Serine-Threonine Kinasesantiproliferative activityapoptosiscolorectal cancerneocryptolepine derivativesPI3K/AKT/mTOR

Identifiers

PMID37894822
PMCPMC10606936
OpenAlexW4387616994

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.