Kronos Bio Data Presentation at EORTC-NCI-AACR Symposium Highlights the Importance of p300 KAT Inhibition in HPV-Driven Tumors
Kronos Bio (NASDAQ: KRON) presented preclinical data from its p300 KAT inhibitor program for HPV-driven tumors at the EORTC-NCI-AACR Symposium. The research demonstrates that their p300 KAT inhibitor, KB-9558, effectively suppresses HPV oncogenes E6 and E7, which are critical for tumor growth. The inhibition leads to restoration of p53 and Rb tumor suppressor pathways, potentially offering a new therapeutic approach for HPV-driven cancers. The study showed that HPV integrates into specific genome locations where p300 regulates transcription, creating a vulnerability that can be targeted by KB-9558.
Kronos Bio (NASDAQ: KRON) ha presentato dati preclinici del suo programma di inibitori della p300 KAT per tumori indotti da HPV al Simposio EORTC-NCI-AACR. La ricerca dimostra che il loro inibitore della p300 KAT, KB-9558, sopprime efficacemente gli oncogeni E6 ed E7 dell'HPV, che sono fondamentali per la crescita tumorale. L'inibizione porta al ripristino delle vie di soppressione tumorale p53 e Rb, offrendo potenzialmente un nuovo approccio terapeutico per i tumori guidati da HPV. Lo studio ha mostrato che l'HPV si integra in posizioni specifiche del genoma dove p300 regola la trascrizione, creando una vulnerabilità che può essere mirata da KB-9558.
Kronos Bio (NASDAQ: KRON) presentó datos preclínicos de su programa de inhibidores de p300 KAT para tumores impulsados por HPV en el Simposio EORTC-NCI-AACR. La investigación demuestra que su inhibidor de p300 KAT, KB-9558, suprime efectivamente los oncogenes E6 y E7 del HPV, que son críticos para el crecimiento tumoral. La inhibición conduce a la restauración de las vías supresoras tumorales p53 y Rb, ofreciendo potencialmente un nuevo enfoque terapéutico para los cánceres impulsados por HPV. El estudio mostró que el HPV se integra en ubicaciones específicas del genoma donde p300 regula la transcripción, creando una vulnerabilidad que puede ser atacada por KB-9558.
Kronos Bio (NASDAQ: KRON)는 EORTC-NCI-AACR 심포지엄에서 HPV 유래 종양을 위한 p300 KAT 억제제 프로그램의 전임상 데이터를 발표했습니다. 연구에 따르면 그들의 p300 KAT 억제제인 KB-9558는 종양 성장에 critical한 HPV 온코겐 E6 및 E7을 효과적으로 억제합니다. 억제 작용은 p53 및 Rb 종양 억제 경로의 복원을 초래하며, HPV 유래 암에 대한 새로운 치료 접근 방식을 제공할 수 있습니다. 이 연구는 HPV가 p300이 전사를 조절하는 특정 유전체 위치에 통합되어 있으며, 이는 KB-9558로 표적화할 수 있는 취약점을 만든다는 것을 보여주었습니다.
Kronos Bio (NASDAQ: KRON) a présenté des données précliniques de son programme d'inhibiteurs de p300 KAT pour les tumeurs à médiation HPV lors du Symposium EORTC-NCI-AACR. La recherche démontre que leur inhibiteur de p300 KAT, KB-9558, supprime efficacement les oncogènes E6 et E7 du HPV, qui sont cruciaux pour la croissance tumorale. L'inhibition conduit à la restauration des voies suppresseurs de tumeur p53 et Rb, offrant potentiellement une nouvelle approche thérapeutique pour les cancers liés au HPV. L'étude a montré que le HPV s'intègre à des emplacements spécifiques du génome où p300 régule la transcription, créant une vulnérabilité pouvant être ciblée par KB-9558.
Kronos Bio (NASDAQ: KRON) hat auf dem EORTC-NCI-AACR-Symposium präklinische Daten ihres p300 KAT-Inhibitorprogramms für durch HPV verursachte Tumoren präsentiert. Die Forschung zeigt, dass ihr p300 KAT-Inhibitor, KB-9558, die HPV-Onkogene E6 und E7, die für das Tumorwachstum entscheidend sind, effektiv unterdrückt. Die Hemmung führt zur Wiederherstellung der Tumorsuppressorwege p53 und Rb und könnte potenziell einen neuen therapeutischen Ansatz für HPV-getriebene Krebserkrankungen bieten. Die Studie zeigte, dass HPV an spezifischen genomischen Orten integriert, an denen p300 die Transkription reguliert, wodurch eine Verwundbarkeit geschaffen wird, die von KB-9558 angesprochen werden kann.
- Preclinical data shows KB-9558 effectively suppresses key tumor-promoting genes E6 and E7
- Demonstrated restoration of critical tumor suppressor pathways (p53 and Rb)
- Identified specific therapeutic vulnerability in HPV-driven tumors
- Research is still in early stages
- No clinical trial data available yet
- Effectiveness in humans remains unproven
Insights
The preclinical data for Kronos Bio's p300 KAT inhibitor (KB-9558) shows promising potential in treating HPV-driven cancers through a novel mechanism. The research demonstrates that p300 KAT inhibition can specifically target HPV oncogenes E6 and E7, which are critical drivers of tumor growth in HPV-related cancers.
The findings are particularly significant because there are currently no approved targeted therapies for HPV-driven tumors. The mechanism of action - restoring p53 and Rb tumor suppressor pathways - is well-validated in cancer biology. The specificity of the approach and the reversibility demonstrated through the control experiments add credibility to the therapeutic potential.
However, investors should note that this is still early-stage preclinical research. The path to clinical trials and potential approval will require significant time and resources, with no guarantee of success. The market opportunity is substantial, considering HPV's role in multiple cancer types including head & neck, cervical and other anogenital cancers.
– Preclinical data demonstrate that inhibiting the p300 KAT domain reactivates p53 in HPV-driven tumors resulting in anti-tumor activity –
SAN MATEO, Calif., and CAMBRIDGE, Mass., Oct. 23, 2024 (GLOBE NEWSWIRE) -- Kronos Bio, Inc. (Nasdaq: KRON), a company dedicated to developing small molecule therapeutics that address cancers and autoimmune diseases driven by deregulated transcription, today announced preclinical data from its p300 KAT inhibitor program for human papillomavirus (HPV)-driven tumors at the EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics.
Kronos Bio is exploring the utility of its p300 KAT inhibitor, KB-9558, for HPV-driven tumors. In the presentation, the authors show that the HPV genome preferentially integrates into transcriptionally active regions in the human genome where it becomes dependent on p300 to drive expression of its E6 and E7 oncogenes. It is widely recognized that elevated transcription of HPV E6 and E7 genes promotes degradation of tumor suppressors p53 and Rb. Importantly, inhibition of p300 KAT activity was highly selective in repressing the transcription of E6 and E7, which in turn led to restoration of the p53 and Rb pathways and drove anti-tumor effects through apoptosis and inhibition of uncontrolled tumor cell growth.
"Continued expression of certain viral genes, especially E6 and E7, plays a critical role in tumor growth and progression of HPV-driven tumors, including head & neck, cervical, and other anogenital cancers. Importantly, there are no approved targeted therapies that inhibit E6 and E7,” said Charles Lin, Ph.D., chief scientific officer of Kronos Bio. "While this is early-stage research, given the ability of p300 KAT inhibition to target E6 and E7 and restore tumor suppressor pathways, we believe this p300 KAT inhibitor has the potential to be a remarkable and unique approach toward ensuring that fewer people suffer from HPV-driven cancer."
In the presentation titled, "Oncogenic human papillomavirus hijacks p300 to drive viral transcription, creating a therapeutic vulnerability that can be exploited with selective p300/CBP catalytic inhibitors", the authors describe the experiments that led to the following key findings:
- HPV integrates into the human genome at specific locations where p300 regulates transcription
- p300 inhibition demonstrated specific and potent reduction of expression of HPV oncogenes E6 and E7, both at the RNA and protein level
- Loss of E6 and E7 led to restoration of p53 and Rb tumor suppressor pathways which led to the upregulation of p53 activated genes (e.g., CDKN1A) and downregulation of Rb repressed genes (e.g., CDK1)
- Re-expression of E6 and E7 from an exogenous lentiviral vector where viral oncogene transcription is not mediated by p300 KAT activity reversed the effects of p300 KAT inhibition on p53 restoration and anti-tumor effects
- These findings support the potential of KB-9558, a p300 KAT inhibitor, to treat HPV-driven tumors given its potential to suppress E6 and E7 expression and restore the p53 pathway
The poster presentation will take place on October 24, 2024, and is currently available under the Publications section of the Kronos Bio website.
About Kronos Bio
Kronos Bio is a clinical-stage biopharmaceutical company dedicated to developing small molecule therapeutics that address deregulated transcription, a hallmark of cancer and autoimmune disease. Our proprietary discovery engine decodes complex transcription factor regulatory networks to identify druggable cofactors. We screen for and optimize small molecules that target these cofactors in a disease-specific context. Kronos Bio has a pipeline of three drug candidates. Istisociclib (KB-0742) is currently enrolling ovarian cancer patients in a Phase 1/2 clinical trial. Preclinical candidate KB-9558 is being developed for multiple myeloma and HPV-driven tumors. KB-7898 is Kronos Bio’s first autoimmune development candidate and has a target indication of Sjögren’s disease. Kronos Bio is based in San Mateo, Calif., and has a research facility in Cambridge, Mass. For more information, visit https://www.kronosbio.com or follow the Company on LinkedIn.
Forward-Looking Statements
Statements in this press release that are not statements of historical fact are forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The press release, in some cases, uses terms such as “anticipate,” “believe,” “could,” “expect,” “plan,” “will,” “may,” or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Forward-looking statements include statements regarding Kronos Bio’s intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things, KB-9558’s ability to potentially treat HPV-driven tumors; the potential of Kronos Bio’s product candidates, pipeline and its proprietary discovery engine; and other statements that are not historical fact. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, including, without limitation: changes in the macroeconomic environment or competitive landscape that impact Kronos Bio’s business; whether Kronos Bio will be able to progress its preclinical pipeline on the timelines anticipated, including due to risks inherent in the development of novel therapeutics; the risk that results of preclinical studies, early clinical trials (including preliminary results) and pharmacokinetic modeling are not necessarily predictive of future results; and risks associated with the sufficiency of Kronos Bio’s cash resources and need for additional capital. These and other risks are described in greater detail in Kronos Bio’s filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in its Quarterly Report on Form 10-Q for the quarter ended June 30, 2024, filed with the SEC on August 8, 2024. Any forward-looking statements that are made in this press release speak only as of the date of this press release and are based on management’s assumptions and estimates as of such date. Except as required by law, Kronos Bio assumes no obligation to update the forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.
FAQ
What is the mechanism of action of Kronos Bio's (KRON) KB-9558 in HPV-driven tumors?
What are the key findings from Kronos Bio's (KRON) October 2024 preclinical data presentation?