A surprising finding reveals key details about how cancer cells metastasize and suggests new therapeutic approaches for halting their spread.
The research centers on a cellular chaperone protein known as GRP78, which helps regulate the folding of other proteins inside cells. Previous studies from the same team have shown that when cells are under stress (due to COVID-19 or cancer), GRP78 gets hijacked, allowing viral invaders to replicate, and cancers to grow and resist treatment.
The researchers have now made an unexpected discovery that may eventually enable scientists to protect cells from that hostile takeover. Typically, GRP78 resides in a part of the cell called the endoplasmic reticulum. But when cells are under stress, the chaperone protein migrates to the cell’s nucleus, where it alters gene activities and changes the behavior of the cell, allowing the cancer cells to become more mobile and invasive.
“Seeing GRP78 in the nucleus controlling gene expression is a total surprise,” said the study’s senior author. “When it comes to the basic mechanisms of cancer cells, this is something novel that, to my knowledge, no one has observed before.”
The findings, just published in the Proceedings of the National Academy of Sciences, could represent a paradigm shift for cell biology, and have implications for cancer therapeutics research, the author said.
To confirm their hypothesis, the researchers used confocal microscopy, which offers high-resolution 2D and 3D imaging, coupled with an advanced technique for capturing images of live cells, to directly observe GRP78 in the nucleus of lung cancer cells, as well as normal cells under stress. They then used several other techniques, including biochemical analysis and mRNA “knock-down” of GRP78. These techniques allowed them to identify the signal within GRP78 that enables it to enter the nucleus and confirm that when GRP78 is present in the nucleus, it stimulates EGFR gene activity.
Next, the researchers set out to learn more about what happens in a cell after GRP78 enters the nucleus. Using a sophisticated form of RNA sequencing they compared lung cancer cells engineered to over-express GRP78 in the nucleus to cells lacking GRP78 in the nucleus in order to learn which genes were affected.
“To our big surprise, we found that the key genes being regulated by GRP78 in the nucleus are mainly involved with cell migration and invasion,” the author said.
The team found that GRP78 binds to ID2, another cellular protein. ID2 typically suppresses genes (including EGFR), many of which allow cells to migrate. But when bound to GRP78, ID2 can no longer do its job. Without that suppression, cancer cells become more invasive.
The new findings point to several potential new approaches for cancer treatment, including down-regulating the activity GPR78 to suppress EGFR in lung cancer, or preventing it from binding to ID2. GRP78 could also bind to other proteins in the nucleus critical for cancer, opening up a new line of research in cancer biology. While the present study analyzed lung cancer cells, GRP78 plays a similar role in various types of cancers, including pancreatic, breast and colon cancer.
The discovery that GRP78, a major endoplasmic reticulum protein, can travel to the nucleus and assume new functions, could also have broad implications across the field of cell biology. The author said it’s possible—even likely—that other proteins that typically reside in one part of the cell could, under stress or other triggers, migrate to another part of the cell and alter cell behavior in multiple ways.
“This is a new concept,” the author said. “The protein itself is the soldier that does the job, but now we’re thinking it’s not just about the soldier, but also where the solider is deployed.”
The team are also studying drugs that can inhibit the expression or activity of GRP78. An ongoing study of theirs suggests that small molecules that inhibit GRP78, such as YUM70, may even be able to block GRP78 activity in the nucleus of cells.
Protein translocation to the nucleus under stress helps cancer cell to migrate
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