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Breast cancer case study could inform clinical trials

Fluorescent microscopy image showing clusters of blue and purple cells on a black background.
Metastatic lesions had far higher levels of MALAT1 (pink) than the surrounding tissues.

When researchers look for potential cancer therapy targets, they typically go after protein-coding genes that participate in disease progression. Disrupt them and negate whatever role they play in cancer’s development or spread. Researchers at Cold Spring Harbor Laboratory (CSHL) have also been working on another kind of target. They’re studying a long non-coding RNA called MALAT1. So far, it’s been linked to more than 20 different types of tumors.

In a new and unique study published in Molecular Therapy: Oncology, CSHL researchers track MALAT1 levels over the course of one woman’s experience with triple-negative breast cancer (TNBC). They find that MALAT1 levels were high at diagnosis and decreased while the patient received standard treatments. Yet, perhaps most importantly, the level increased at a distant metastatic site. The researchers see this as supporting a role for MALAT1 in TNBC’s spread.

The study allowed CSHL to interrogate this potential treatment target like never before. “Even though MALAT1 has been implicated in different cancers, including breast cancer, nobody has looked at how MALAT1 levels change over treatment and disease progression,” says Disha Aggarwal, the graduate student who spearheaded the study.

Diagram showing cancer progression, treatment stages, and graph of MALAT1 intensity in stroma and metastatic lesions.
As illustrated here, levels of MALAT1 were highest at initial diagnosis and in a distant metastatic site. The finding suggests that MALAT1 plays a role in enabling triple-negative breast cancer to spread throughout the body.

Researchers examined tissue samples from a 59-year-old woman diagnosed with stage 1 TNBC. The patient underwent different treatments over two and a half years, including surgery, chemotherapy, radiation, and immunotherapy. After a period of regression, the cancer became metastatic. Unfortunately, three and a half years after diagnosis, the individual succumbed to the disease. However, what she left behind will hopefully help others.

Studying tissue samples from throughout the course of treatment and disease progression presented a rare opportunity, says CSHL Professor David Spector. “Researchers typically get to see an initial sample and an end sample, but not progressive samples in the depth that we were able to look at here.” What they’ve seen may eventually inform future treatments.

Since 2015, the Spector lab has been collaborating with Ionis Pharmaceuticals to develop a drug targeting MALAT1. They’re now speaking with biotech companies in hopes of launching a clinical trial within the next few years. But that’s not all.

Spector’s lab is also exploring whether MALAT1 could enable doctors to predict the risk of someone’s cancer recurring or becoming metastatic. If so, it could not only guide therapeutic strategies for women who have been diagnosed with TNBC. It could factor in for those with more common and less severe forms of breast cancer.

Written by: Jen A. Miller | publicaffairs@cshl.edu | 516-367-8455


Funding

National Institutes of Health, National Cancer Institute, CSHL-Northwell Health Affiliation

Citation

Aggarwal, D., et al., “Longitudinal tracking of MALAT1 level over a breast cancer patient’s course of treatment and disease progression”, Molecular Therapy: Oncology, October 17, 2025. DOI: 10.1016/j.omton.2025.201070

Core Facilites

image of the microscopy core facility icon “The Microscopy Core Facility provides training, consultation, experimental design and technical assistance to investigators at CSHL in widefield, spinning disk laser scanning or point laser scanning confocal fluorescence microscopy, and super-resolution microscopy. In addition, the Microscopy Shared Resource provides customized state-of-the-art optical imaging and quantitative image analysis applications to support a wide range of scientific endeavors.” — Director Erika Wee, Ph.D.

Animal Tissue Imaging “The Tissue Imaging Shared Resource provides a spectrum of on-demand and researcher-tailored histopathological services, including tissue sampling, processing, embedding, and sectioning, as well as H&E, special, and immunohistochemistry staining. We not only support laser-capture microdissection and whole-slide scanning, but also offer histopathology consultation and instrument training.” — Manager Kristin Milicich

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Principal Investigator

David L. Spector

David L. Spector

Professor
Robert B. Gardner Jr., Professor
Cancer Center Member
Ph.D., Rutgers University, 1980

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