CancerNeuroscience: Systematic dissection of the crosstalk between cancer and the nervous system
Lead Research Organisation:
The Francis Crick Institute
Department Name: Research
Abstract
Accumulating evidence has indicated a crucial role of the nervous system in cancer. Changes of the innervation landscape, significantly impacting cancer progression, have been observed in many cancer types. However, perturbations of neural activity have yielded incoherent results in distinct cancer types, and sometimes even in the same cancer type across different studies. This variability may be due to the limitations in the currently employed methodologies: the composition of cancer-innervating neurons has not been extensively profiled, and the standard methods used to manipulate neural activity, such as surgical denervation and pharmacological treatment, lack specificity and selectivity in both the location of the perturbation and types of neurons affected, which complicates the interpretation of results.
On the basis of current evidence, we hypothesise that different subsets of neurons have distinct impact on cancer progression; therefore, selective manipulation of specific subsets of cancer-innervating neurons will be crucial to illustrate their functional roles in tumourigenesis. To overcome the limitations of the conventional approaches, we will systematically dissect the crosstalk between cancer and the nervous system by interrogating a panel of genetically engineered mouse models of cancer with contemporary neuroscience methodologies. We will first perform anatomic and molecular characterisation of tumour-innervating neurons, followed by functional investigation using well-established genetic tools, including optogenetics and chemogenetics, which will allow cell-type-and circuit-specific perturbations of neural activity at temporal and spatial resolutions that cannot be achieved by conventional surgical or pharmacological methods.
With this cross-disciplinary approach, we aim to unveil potential common logic underlying the involvement of the nervous system in cancer progression, which may ultimately lead to breakthroughs in clinical cancer treatment.
On the basis of current evidence, we hypothesise that different subsets of neurons have distinct impact on cancer progression; therefore, selective manipulation of specific subsets of cancer-innervating neurons will be crucial to illustrate their functional roles in tumourigenesis. To overcome the limitations of the conventional approaches, we will systematically dissect the crosstalk between cancer and the nervous system by interrogating a panel of genetically engineered mouse models of cancer with contemporary neuroscience methodologies. We will first perform anatomic and molecular characterisation of tumour-innervating neurons, followed by functional investigation using well-established genetic tools, including optogenetics and chemogenetics, which will allow cell-type-and circuit-specific perturbations of neural activity at temporal and spatial resolutions that cannot be achieved by conventional surgical or pharmacological methods.
With this cross-disciplinary approach, we aim to unveil potential common logic underlying the involvement of the nervous system in cancer progression, which may ultimately lead to breakthroughs in clinical cancer treatment.
People |
ORCID iD |
| Leanne Li (Principal Investigator) |
Publications
Peinado P
(2025)
Intrinsic electrical activity drives small-cell lung cancer progression.
in Nature
| Description | - We found that certain highly aggressive lung cancer cells are electrically active, like neurons, and such electrical activity directly promotes cancer progression. - We found that lung cancers recruit nerves to grow around them, and the crosstalk between cancer and their surrounding nerve cells may promote cancer development. - Changing the nerve density around the tumours alters the immune reactions against the cancer. - Metabolic symbiosis between heterogeneous cancer cells promotes the electrical activity and aggressiveness of neuroendocrine cancer cells |
| Exploitation Route | New drugs or repurposed drugs could be developed and tested for treatment of one of the most lethal types of lung cancer, the therapeutic landscape of which remained relatively unchanged for the past forty years. |
| Sectors | Healthcare Pharmaceuticals and Medical Biotechnology |
| Description | Our lab has participated in several outreach and philanthropy events, in which we talked about our new discoveries arising from the award. The audience were very enthusiastic and engaged, because they've never heard of this emerging area of research. Both young students and philanthropists reached out to express their interest in our research. |
| Description | Clinical collaboration |
| Organisation | National Taiwan University Hospital |
| Country | Taiwan, Province of China |
| Sector | Hospitals |
| PI Contribution | We recognize them as co-authors in our papers. |
| Collaborator Contribution | We obtain clinical samples from our collaborating clinicians. |
| Impact | Part of the collaboration has resulted in the Nature paper we published. Will have more manuscripts coming up. |
| Start Year | 2024 |
| Description | Clinical collaboration |
| Organisation | University of Texas Southwestern Medical Center |
| Country | United States |
| Sector | Academic/University |
| PI Contribution | We recognize them as co-authors in our papers. |
| Collaborator Contribution | We obtain clinical samples from our collaborating clinicians. |
| Impact | Part of the collaboration has resulted in the Nature paper we published. Will have more manuscripts coming up. |
| Start Year | 2024 |
| Description | Electrophysiology collaboration |
| Organisation | University of Cambridge |
| Department | Department of Physiology, Development and Neuroscience |
| Country | United Kingdom |
| Sector | Academic/University |
| PI Contribution | Provide cancer cell lines and animal models. |
| Collaborator Contribution | Help to establish patch clamp protocols in cancer cells. |
| Impact | This collaboration has resulted in the Nature paper we just published. |
| Start Year | 2013 |
| Description | Interview with journalists |
| Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
| Part Of Official Scheme? | No |
| Geographic Reach | National |
| Primary Audience | Media (as a channel to the public) |
| Results and Impact | Journalists visited and chatted about our ongoing research. Some of them resulted in press release while others remain unknown. |
| Year(s) Of Engagement Activity | 2022,2023,2024,2025 |
| Description | Philanthropy events |
| Form Of Engagement Activity | Participation in an open day or visit at my research institution |
| Part Of Official Scheme? | No |
| Geographic Reach | National |
| Primary Audience | Supporters |
| Results and Impact | Participated in CRUK events to meet with potential donors. |
| Year(s) Of Engagement Activity | 2021,2022,2023,2024 |
| Description | Visit of the shadow cabinet |
| Form Of Engagement Activity | Participation in an open day or visit at my research institution |
| Part Of Official Scheme? | No |
| Geographic Reach | National |
| Primary Audience | Policymakers/politicians |
| Results and Impact | N/A |
| Year(s) Of Engagement Activity | 2025 |