Effects ofCallicarpa nudifloraGranules on the Proliferation and Apoptosis of Uterine Fibroid Cells
article
OA: closed
CC0
Abstract
This research was aimed to discuss and understand the effects and mechanisms of action of Callicarpa nudiflora granules on proliferation and apoptosis of uterine leiomyoma (UL) cells. Firstly, normal uterine myometrium (UM) and UL tissues were collected, and the levels of p-Akt and Phosphatase and Tensin Homolog (PTEN) in UL tissues were detected using immunohistochemistry. Next, the UL cells were successfully obtained using enzymatic digestion, and their identification was performed using alpha-smooth muscle actin ( α -actin) immunocytochemistry. Specifically, the cells were grouped into four: a control group (CG), a low-dose group (LDG, 50 mg/L Callicarpa nudiflora solution), a medium-dose group (MDG, 100 mg/L Callicarpa nudiflora solution), and a high-dose group (HDG, 200 mg/L Callicarpa nudiflora solution). Moreover, the proliferation of UL cells was assessed using the thiazolyl blue (MTT) assay, while cell apoptosis was analyzed using flow cytometry (FCT). Real-time fluorescent quantitative PCR (fq-PCR) and Western blot assay (WBA) were utilized to determine the PAI-1, P38, TGF- β 1, E-cadherin, and Vimentin in UL cells. The results revealed that the positive rate (PR) of p-Akt in the UL tissues was much higher to that in normal UM tissues ( P < 0.001). More than 90% of UL cells were positive for α -actin. The viabilities of UL cells in the Callicarpa nudiflora treatment groups were greatly weakened to that of untreated cells ( P < 0.05). Viability of UL cells in the HDG group was the lowest, showing a great difference with P < 0.01 to the LDG group and that with P < 0.05 to the MDG group, while that between the MDG and LDG groups exhibited a great difference with P < 0.05. AR of UL cells in CG group was sharply lower to that in the Callicarpa nudiflora treatment groups, showing great differences with P < 0.05, P < 0.01, and P < 0.001, respectively. AR of UL cells in HDG group was higher to the LDG group ( P < 0.01) and MDG group ( P < 0.05), and that in LDG group was lower and exhibited a great difference with P < 0.05 to the MDG group. The HDG, LDG, and MDG groups exhibited greatly lower TGF- β 1, PAI-1, and P38 to the CG group ( P < 0.05). In the HDG group, the TGF- β 1, PAI-1, P38, and Vimentin levels were greatly lower and presented a great difference with P < 0.01 to those in the CG group and LDG group. Additionally, E-cadherin in UL cells was elevated in the LDG and MDG groups to CG group, showing P < 0.05 and P < 0.01, respectively. Such findings indicated that the Callicarpa nudiflora granules can suppress proliferation of UL cells and promote their apoptosis, which may be associated with the TGF- β 1/P38/PAI-1 singling pathway (SPW).
My notes (saved in your browser only)
Citation neighborhood (sparse)
Too few in-corpus citations on either side for a chart; here are the lists.
Cites (1)
References (37)
- Nodal induces apoptosis and inhibits proliferation in ovarian endometriosis-clear cell carcinoma lesions via openalex
- W2540186553 via openalex
- W2560728740 via openalex
- W2606062902 via openalex
- W2734801691 via openalex
- W2770132733 via openalex
- W2771421514 via openalex
- W2914196959 via openalex
- W2971488563 via openalex
- W2981632129 via openalex
- W2995568109 via openalex
- W2998878953 via openalex
- W3012001797 via openalex
- W3026325224 via openalex
- W3048034328 via openalex
- W3082344045 via openalex
- W3082851906 via openalex
- W3127005116 via openalex
- W3134800206 via openalex
- W3135736296 via openalex
- W3172746379 via openalex
- W3186998543 via openalex
- W3200688082 via openalex
- W3207391497 via openalex
- W4200501724 via openalex
- W4205396212 via openalex
- W4220706939 via openalex
- W4221123479 via openalex
- W4281263904 via openalex
- W4281552734 via openalex
- W4283369591 via openalex
- W4294783232 via openalex
- W4308680514 via openalex
- W4312305937 via openalex
- W6769929043 via openalex
- W2041366267 via openalex
- W6840832826 via openalex
Source provenance
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
License: CC0
· commercial use OK