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Updated: Jan 6, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Druggable Molecular Targets for the Treatment of Triple Negative Breast Cancer
Maryam Nakhjavani1,2, Jennifer E Hardingham1,2, Helen M Palethorpe1,2
1Molecular Oncology, Basil Hetzel Institute, The Queen Elizabeth Hospital, Woodville South, Australia.
Abstract:
Breast cancer (BC) is still the most common cancer among women worldwide. Amongst the subtypes of BC, triple negative breast cancer (TNBC) is characterized by deficient expression of estrogen, progesterone, and human epidermal growth factor receptor 2 receptors. These patients are therefore not given the option of targeted therapy and have worse prognosis as a result. Consequently, much research has been devoted to identifying specific molecular targets that can be utilized for targeted cancer therapy, thereby limiting the progression and metastasis of this invasive tumor, and improving patient outcomes. In this review, we have focused on the molecular targets in TNBC, categorizing these into targets within the immune system such as immune checkpoint modulators, intra-nuclear targets, intracellular targets, and cell surface targets. The aim of this review is to introduce and summarize the known targets and drugs under investigation in phase II or III clinical trials, while introducing additional possible targets for future drug development. This review brings a tangible benefit to cancer researchers who seek a comprehensive comparison of TNBC treatment options.
Insights
Triple-negative breast cancer (TNBC) lacks targeted therapies, driving research into new molecular targets. This review summarizes current TNBC targets and drugs in clinical trials for improved patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) is the most common breast cancer subtype in women globally.
- TNBC is defined by the absence of estrogen, progesterone, and HER2 receptors, limiting targeted therapy options.
- Patients with TNBC often face a poorer prognosis compared to other breast cancer subtypes.
Purpose of the Study:
- To review and summarize molecular targets for TNBC.
- To categorize identified targets into immune, intra-nuclear, intracellular, and cell surface categories.
- To provide a comprehensive overview of current and potential TNBC therapeutic targets.
Main Methods:
- Literature review focusing on molecular targets in TNBC.
- Categorization of targets based on their cellular location or function.
- Inclusion of drugs currently in Phase II or III clinical trials.
Main Results:
- Identified and categorized various molecular targets within the immune system (e.g., immune checkpoint modulators), intracellularly, intra-nuclearly, and on the cell surface.
- Summarized drugs under investigation for TNBC in ongoing clinical trials.
- Highlighted potential novel targets for future drug development.
Conclusions:
- Effective targeted therapies for TNBC are urgently needed due to its aggressive nature and limited treatment options.
- The identified molecular targets represent promising avenues for developing novel TNBC therapies.
- This review offers valuable insights for researchers seeking to advance TNBC treatment strategies.
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