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Shapeshifting cancers' masters, unmasked


News provided by

Cold Spring Harbor Laboratory

Nov 24, 2025, 07:30 ET

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COLD SPRING HARBOR, N.Y., Nov. 24, 2025 /PRNewswire/ -- Some tumors are almost impossible to treat. That's especially true for carcinomas, which don't behave like other malignancies. Some of these tumors act as shapeshifters and start to resemble cells from other organs of the human body, such as skin. This bizarre behavior presents a challenge for existing therapies. "The tumors are notoriously plastic in their cellular identity," says Cold Spring Harbor Laboratory (CSHL) Professor Christopher Vakoc. Some may even change to escape cancer treatment.

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A new study from the Vakoc lab reveals how tuft cell lung cancer’s master regulator, POUF23, binds to DNA and the OCA-T1 protein. The crystal structure of this three-part interface, seen here from the front and back, allows scientists to consider how and which kinds of drugs might target it. The study’s first author, former postdoc Aktan Alpsoy, is now a faculty member at Middle East Technical University.
A new study from the Vakoc lab reveals how tuft cell lung cancer’s master regulator, POUF23, binds to DNA and the OCA-T1 protein. The crystal structure of this three-part interface, seen here from the front and back, allows scientists to consider how and which kinds of drugs might target it. The study’s first author, former postdoc Aktan Alpsoy, is now a faculty member at Middle East Technical University.

Recent studies from the Vakoc lab shine a new light on two hard-to-treat carcinomas, revealing vulnerabilities that could "tee up targets for therapy," he says.

In a study published in Nature Communications, CSHL researchers identify a protein that determines whether pancreatic cancer cells maintain their classical form or begin to look and act more like skin cells. Meanwhile, in Cell Reports, they uncover the crystal structure of another group of proteins that plays a key role in tuft cell lung cancer.

This latest finding represents a full-circle moment for the lab, Vakoc explains. When he and his colleagues discovered tuft cell lung cancer in 2018, they were searching for epigenetic factors that drive tumor growth. In other words, they were looking beyond the genes themselves and into the processes of transcription and gene regulation. Now, in collaboration with CSHL Director of Research Leemor Joshua-Tor, they've found what could someday become an epigenetic therapy designed to stop the cancer's growth.

Together, the two new studies continue to build on one of Vakoc's main goals of the last 17 years. "We aim to identify the master regulators of cellular identity," he says. The hope is that these "master regulators" could someday become the targets of new medicines, much like hormone therapies now used against breast and prostate cancers that were once difficult to treat. Of course, there's still a long way to go.

Should the findings eventually lead to new drugs, Vakoc hopes they will be engineered to target the cancer without harming other parts of the patient's body. That ethos is apparent in both of his lab's latest studies. Whether going after mouse models of pancreatic cancer or lung cancer, they see no evidence of toxicity or damage to vital organs. "We're setting a higher bar for specificity when it comes to new cancer targets and treatments," Vakoc says.

They're not just working toward new medicines. They're coming to a deeper understanding of cellular identity, and in so doing, they're helping establish a new and better standard of care.

About Cold Spring Harbor Laboratory
Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,000 people including 600 scientists, students and technicians. For more information, visit www.cshl.edu.

SOURCE Cold Spring Harbor Laboratory

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