Evidence map›Paper›PMID 39544485›Full record

ArticleAdvances in pharmacological and pharmaceutical sciences2024

Saikosaponin-b2 Regulates the Proliferation and Apoptosis of Liver Cancer Cells by Targeting the MACC1/c-Met/Akt Signalling Pathway.

Yanxue Zhu, Xingzhi Lv, Ruifang Li, Zihan Gao, Chanhao Lei, Lan Wang, Sanqiang Li

Abstract read
In one paragraph

Article in Advances in pharmacological and pharmaceutical sciences, 2024. 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
–field-weighted citation impact
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.

  1. Review
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

7 authors.

Yanxue ZhuDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.
Xingzhi LvDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.
Ruifang LiDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.ORCID https://orcid.org/0000-0002-1861-1809
Zihan GaoDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.
Chanhao LeiDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.
Lan WangDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.
Sanqiang LiDepartment of Pharmacology, Basic Medicine and Forensic Medicine College, Henan University of Science and Technology, KaiYuan Road 263, Luoyang 471023, Henan, China.ORCID https://orcid.org/0000-0001-8452-8205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Saikosaponin-b2 (SS-b2), an active ingredient derived from the root of Radix Bupleuri, possesses antitumour, anti-inflammatory, antioxidative and hepatoprotective properties. We investigated the inhibition of tumour proliferation by SS-b2 and the underlying molecular mechanisms, including the MACC1/p-c-Met/p-Akt pathway expression in HepG2 liver cancer cells and H22 tumour-bearing mice. Animal experiments showed that SS-b2 significantly decreased the levels of MACC1, p-c-MET and p-Akt in tumour tissue transplanted with H22 liver cancer cells in mice, while it increased the expression of p-BAD. The results also revealed a concentration-dependent suppression of MACC1, p-c-Met and p-Akt expression in the SS-b2 treatment group compared with the control group. Additionally, the suppression of MACC1 activation by SS-b2 resulted in a reduction in the viability and proliferation of HepG2 liver cancer cells, and this reduction was comparable to that by doxorubicin (DOX). This suggests that SS-b2 has significant efficacy in liver cancer, comparable to DOX. Meanwhile, Annexin V-FITC/PI staining and western blot analysis of cleaved caspase 9 and cleaved caspase 3 demonstrated that SS-b2 induced apoptosis of HepG2 liver cancer cells. These findings provide experimental evidence suggesting that SS-b2 is a promising anticancer agent for liver cancer.

Indexed as

c-Met signallingliver cancermetastasis-associated in colon cancer-1saikosaponin-b2

Identifiers

PMID39544485
PMCPMC11561180

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