
CYRI-B, a regulator of RAC1 and macropinocytosis, controls the internalisation of the lysophosphatidic acid receptor LPAR1, thereby modulating chemotactic migration and metastasis in pancreatic cancer.


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Pancreatic ductal adenocarcinoma carries a dismal prognosis, with high rates of metastasis and few treatment options. Hyperactivation of KRAS in almost all tumours drives RAC1 activation, conferring enhanced migratory and proliferative capacity as well as macropinocytosis. Macropinocytosis is well understood as a nutrient scavenging mechanism, but little is known about its functions in trafficking of signaling receptors. We find that CYRI-B is highly expressed in pancreatic tumours in a mouse model of KRAS and p53- driven pancreatic cancer. Deletion of CYRI-B accelerates tumourigenesis, leading to enhanced ERK and JNK-induced proliferation in precancerous lesions, indicating a role as a buffer of RAC1 hyperactivation in early stages. However, as disease progresses, loss of CYRI-B inhibits metastasis. CYRI-B depleted tumour cells show reduced chemotactic responses to lysophosphatidic acid, a major driver of tumour spread, due to impaired macropinocytic uptake of LPAR1 receptor. Overall, we implicate CYRI-B as a mediator of growth and signaling in pancreatic cancer, providing new insights into pathways controlling metastasis.

### Competing Interest Statement

The authors have declared no competing interest.

CYRI-B mediated macropinocytosis drives metastasis via lysophosphatidic acid receptor uptake

cyri-b-regulates-macropinocytic-uptake-of-lpar1-to-control-metastasis-in-pancreatic-cancer


CYRI-B Regulates Macropinocytic Uptake of LPAR1 to Control Metastasis in Pancreatic Cancer
