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Updated: Jul 27, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
LEM Domain Containing 1 Acts as a Novel Oncogene and Therapeutic Target for Triple-Negative Breast Cancer
Xiangling Li1,2, Shilong Jiang3, Ting Jiang1
1Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, China.
Abstract:
Breast cancer is the most common deadly malignancy in women worldwide. In particular, triple-negative breast cancer (TNBC) exhibits the worst prognosis among four subtypes of breast cancer due to limited treatment options. Exploring novel therapeutic targets holds promise for developing effective treatments for TNBC. Here, we demonstrated for the first time that LEMD1 (LEM domain containing 1) is highly expressed in TNBC and contributes to reduced survival in TNBC patients, through analysis of both bioinformatic databases and collected patient samples. Furthermore, LEMD1 silencing not only inhibited the proliferation and migration of TNBC cells in vitro, but also abolished tumor formation of TNBC cells in vivo. Knockdown of LEMD1 enhanced the sensitivity of TNBC cells to paclitaxel. Mechanistically, LEMD1 promoted the progress of TNBC by activating the ERK signaling pathway. In summary, our study revealed that LEMD1 may act as a novel oncogene in TNBC, and targeting LEMD1 may be exploited as a promising therapeutic approach to enhance the efficacy of chemotherapy against TNBC.
Insights
LEMD1 is highly expressed in triple-negative breast cancer (TNBC), contributing to poor survival. Targeting LEMD1 shows promise for improving TNBC treatment and chemotherapy efficacy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) presents a significant clinical challenge due to limited therapeutic options and poor patient survival rates.
- Identifying novel therapeutic targets is crucial for advancing TNBC treatment strategies.
Purpose of the Study:
- To investigate the role of LEM domain containing 1 (LEMD1) as a potential therapeutic target in triple-negative breast cancer.
- To elucidate the mechanism by which LEMD1 influences TNBC progression and patient outcomes.
Main Methods:
- Bioinformatic analysis of public databases and patient samples to assess LEMD1 expression in TNBC.
- In vitro studies involving LEMD1 silencing to evaluate its impact on TNBC cell proliferation and migration.
- In vivo tumor formation assays and chemosensitivity tests to assess the therapeutic potential of targeting LEMD1.
Main Results:
- LEMD1 was found to be highly expressed in TNBC tissues and correlated with reduced patient survival.
- LEMD1 silencing significantly inhibited TNBC cell proliferation, migration, and in vivo tumor growth.
- Knockdown of LEMD1 increased the sensitivity of TNBC cells to paclitaxel chemotherapy.
- LEMD1 promotes TNBC progression by activating the ERK signaling pathway.
Conclusions:
- LEMD1 functions as a novel oncogene in triple-negative breast cancer.
- Targeting LEMD1 represents a promising therapeutic strategy to improve treatment outcomes and enhance chemotherapy efficacy in TNBC.
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