Evidence map›Paper›PMID 38874684›Full record

ArticleBreast cancer research and treatment2024

UM171 suppresses breast cancer progression by inducing KLF2.

Xiaojuan Ran, Anling Hu, Yi Kuang, Chunlin Wang, Wuling Liu, Xiao Xiao, Eldad Zacksenhaus, Xiangdi Yu, Yaacov Ben-David

Abstract read
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Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Xiaojuan Ran *Guizhou University of Traditional Chinese Medicine, Guiyang, China.
Anling Hu *State Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China.
Yi KuangState Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China.
Chunlin WangState Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China.
Wuling LiuState Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China.
Xiao XiaoState Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China.
Eldad ZacksenhausDepartment of Medicine, Laboratory Medicine & Pathobiology and Medical Biophysics, University of Toronto, Toronto, ON, M5G 1L1, Canada.
Xiangdi YuGuizhou University of Traditional Chinese Medicine, Guiyang, China. Xiangdi_Yu@163.com.
Yaacov Ben-DavidState Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, Guizhou, People's Republic of China. yaacovbendavid@hotmail.com.

Funding

Guangzhou Provincial Medical Science Basic Research B2023047Guizhou Provincial High level creative talents cultivation plan: Thousand plan GZSYQCC [2016]001Guizhou Provincial Natural Science Foundation of China Qiankehejichu-ZK [2021] Zhongdian006the Guizhou Administration of Traditional Chinese Medicine (QZYY-2024-023)the National Natural Science Foundation of China 82060239the National Natural Science Foundation of China U1812403the Open Grant from State Key Laboratory for Functions and Applications of Medicinal Plants of Guizhou Medical University QJHKYZ [2022]391the Science and Technology Department of Guizhou Province (QKHJC-ZK[2024] Yiban 641)the Science and Technology Department of Guizhou Province Grants QKHJC-ZK [2022]YB297the Science and Technology Department of Guizhou Province Grants QKHJC-ZK[2023]YB240
6 · The paper itself

Abstract

purposeBreast cancer is the most frequent cancer in women with significant death rate. Morbidity is associated with drug resistance and metastasis. Development of novel drugs is unmet need. The aim of this study is to show potent anti-neoplastic activity of the UM171 compound on breast cancer cells and its mechanism of action.

methodsThe inhibitory effect of UM171 on several breast cancer (BC) cell lines was examined using MTT and colony-forming assays. Cell cycle and apoptosis assays were utilized to determine the effect of UM171 on BC cell proliferation and survival. Wound healing scratch and transwell migration assays were used to examine the migration of BC cell lines in culture. Xenograft of mouse model with 4T1 cells was used to determine inhibitory effect of UM171 in vivo. Q-RT-PCR and western blotting were used to determine the expression level of genes effected by UM171. Lentivirus-mediated shRNAs were used to knockdown the expression of KLF2 in BC cells.

resultsUM171 was previously identified as a potent agonist of human hematopoietic stem cell renewal and inhibitor of leukemia. In this study, UM171 was shown to inhibit the growth of multiple breast cancer cell lines in culture. UM171-mediated growth inhibition was associated with the induction of apoptosis, G2/M cell cycle arrest, lower colony-forming capacity, and reduced motility. In a xenotransplantation model of mouse triple-negative breast cancer 4T1 cells injected into syngeneic BALB/c mice, UM171 strongly inhibited tumor growth at a level comparable to control paclitaxel. UM171 increased the expression of the three PIM genes (PIM1-3) in breast cancer cells. Moreover, UM171 strongly induced the expression of the tumor suppressor gene KLF2 and cell cycle inhibitor P21

conclusionThese results suggested that UM171 inhibited breast cancer progression in part through activation of KLF2 and P21. Combination of UM171 with a PAN-PIM inhibitor offer a novel therapy for aggressive forms of breast cancer.

Indexed as

ApoptosisBreast NeoplasmsCell MovementCell ProliferationKruppel-Like Transcription FactorsXenograft Model Antitumor AssaysAnimalsAntineoplastic AgentsCell Line, TumorDisease Models, AnimalDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMiceAntineoplastic AgentsKLF2 protein, humanKruppel-Like Transcription FactorsBreast cancerKLF2P21PIM1-PIM3 activationProliferationUM171

Identifiers

PMID38874684
PMCPMC11297059

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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.