Tumor cells shown to enter bloodstream from deep within early–stage tumors.
The scientists at The Scripps Research Institute (TSRI) have discovered why some cancers may reoccur after years in remission.

The findings, published recently in the journal Cell Reports, show that invasive tumors can begin sending out tumor cells far earlier than previously thought. These escaping cells – which can enter the bloodstream before the primary tumor is detected – may seed secondary tumors that don’t show up for years.

Importantly, the scientists demonstrated that the escaping tumor cells reach the bloodstream by entering blood vessels deep within the dense tumor core, upending the long–held belief that metastatic cells come from a tumor’s invasive borders.

“The actual process of cancer cell dissemination via hematogenous routes is a relatively under–studied process, but we finally have an answer as to where it takes place,” said TSRI Assistant Professor Elena Deryugina, who led the study in a long–term collaboration with TSRI Staff Scientist William Kiosses.

Using cancer cell lines generated from human fibrosarcoma and carcinoma tumors, the researchers found that primary tumors can send out cells early on – independent of cancer invasion into adjacent tissue. This could explain why doctors often see secondary tumors appearing earlier than they would have predicted.

This finding may also shed light on why patients with early stage tumors still have a risk of developing metastatic disease. “These metastases may have been seeded when the primary tumor was even too small to be visualized,” Deryugina said.

Peering through dense primary tumors had been a roadblock in cancer studies until now, and this new discovery was possible because the researchers developed of animal models that allowed for microscopic analysis of tumor cell dissemination. Specifically, adapted mouse ear and chick embryo models let the scientists examine developing tumors through relatively thin tissue layers.

The new study is also the first to examine entire tumors to find out exactly where escaping cells come from. The scientists tagged human tumor cells with a florescent protein to distinguish them from the cells of a tumor–bearing animal. Using high–resolution confocal microscopy techniques spearheaded by Kiosses, the researchers mapped in 3–D all blood vessels across entire tumors, from the tumors’ dense cores to their invasive tendrils.

The researchers mapped the location of every tumor cell relative to the center of the closest blood vessel – or visualized within blood vessels. This approach gave the researchers a way to finally analyze the escape process, called intravasation, and to demonstrate where intravasating cells enter blood vessels.

The researchers were surprised by what they found: The vast majority of tumor cells entered blood vessels within the tumor core, not in the invasive tendrils.

This discovery challenges the long–held assumption that tumor cells enter the bloodstream only after they invade adjacent stroma and reach tumor–converging blood vessels. Instead, the researchers found that fewer than 10 percent of escaped cells intravasated from the stroma–invading sprouts. The researchers also found that levels of a protein called EGFR could be a good indicator of whether tumor cells would intravasate. EGFR appeared to regulate a tumor’s ability to induce blood vessels that support cancer cell escape. “Therefore, the data indicate the importance of harnessing the EGFR activity early on in cancer patients,” said Deryugina.

Next, the researchers plan to investigate the functional roles of different cell types within a primary tumor, such as inflammatory leukocytes, which also may be critically important for supporting intratumoral cancer cell intravasation.