CDK4/6 inhibitors in combination with anti-oestrogens have prolonged survival of patients with oestrogen receptor (ER)-positive/HER2-negative metastatic breast cancer. However, this combination is not curative, mainly due to acquired drug resistance. Knowledge about mechanisms of such resistance remains incomplete. Dr Dhivya Sudhan (UT Southwestern Medical Center, TX, USA) reported results of new insights in the pathways leading to CDK4/6 inhibitor resistance [1].
Using CRISPR/Cas9 to delete the DNA mismatch repair gene MSH2 in MCF7 and T47D ER-positive breast cancer cells, Dr Sudhan and colleagues obtained cells with drug resistance-associated mutations. Clones resistant to CDK4/6 inhibitors were selected and subjected to whole exome sequencing. Of the 10 genes recurrently mutated in the CDK4/6 inhibitor resistant cells, loss of ASXL1 tumour suppressor was identified as top hit. Loss of ASXL1 has been implicated in myeloid transformation through epigenetic reprogramming. In line with these findings, among 1,769 tumours from patients treated with CDK4/6 inhibitor (TEMPUS database), 37 exhibited ASXL1 alterations. In addition, RNA sequencing of patient-derived organoids established from post-CDK4/6 inhibitor metastases, identified ASXL1 mutations in 2/7 organoids (29%). Functional studies showed that loss of ASXL1 was associated with maintenance of retinoblastoma phosphorylation in the presence of CDK4/6 inhibition, markedly higher levels of CDK2, CDK6, cyclins E and A, and downregulation of p21 and p27.
“We identified loss of ASXL1 as a novel mechanism of resistance to CDK4/6 inhibition,” concluded Dr Sudhan. “Knockdown of CDK2 and cyclin A restored sensitivity to CDK4/6 inhibitors and reduced viability of ASXL1 deficient cells, suggesting that CDK2 inhibitors are a treatment approach against these drug-resistant tumours.”
- Sudhan DR, et al. Loss of ASXL1 tumor suppressor promotes resistance to CDK4/6 inhibitors in ER+ breast cancer. GS3-09, SABCS 2021 Virtual Meeting, 7–10 December.
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Table of Contents: SABCS 2021
Featured articles
Early-Stage Breast Cancer
Aromatase inhibitors outperform tamoxifen in premenopausal women
Concurrent taxane plus anthracycline most beneficial in reducing risk of breast cancer
Reduced risk of recurrence with ovarian suppression plus tamoxifen/exemestane
Metformin does not improve outcomes in patients with early-stage breast cancer
Omitting sentinel lymph node biopsy improves arm symptoms
HR-positive/HER2-negative Breast Cancer
Addition of palbociclib to standard endocrine therapy does not improve outcome in adjuvant treatment
The SERD elacestrant improves outcomes for patients unresponsive to endocrine therapy
Consistent overall survival benefit of ribociclib in advanced breast cancer
Premenopausal women benefit from adjuvant chemotherapy next to endocrine therapy
Promising anti-tumour activity of the CDK7-inhibitor samuraciclib plus fulvestrant
ctDNA is prognostic and predictive for response to ribociclib plus letrozole
Early switch to fulvestrant plus palbociclib beneficial for patients with ESR1 mutation
Triple-Negative Breast Cancer
Single-cell spatial analysis can predict response to neoadjuvant immunotherapy
Neoadjuvant pembrolizumab plus chemotherapy benefits event-free survival in TNBC
Early use of ctDNA testing can identify likelihood of relapse in TNBC
Pembrolizumab plus chemotherapy benefits patients with combined positive score ≥10
Neratinib plus trastuzumab plus fulvestrant shows encouraging clinical activity
Phase 1–3 Trials
Datopotamab deruxtecan shows promising anti-tumour activity
Trastuzumab deruxtecan outperforms trastuzumab emtansine
Nivolumab plus ipilimumab serve promising dual checkpoint inhibition
Entinostat plus exemestane improves progression-free survival in Chinese patients
Efficacy of pyrotinib plus capecitabine confirmed in previously treated patients
Basic and Translational Research
Using genomics to match treatments improves outcomes
Loss of ASXL1 tumour suppressor promotes resistance to CDK4/6 inhibitors
Inducers of ferroptosis are potential drugs to target p53-mutated TNBC cells
MAPK-pathway alterations are associated with resistance to anti-HER2 therapy
Genomic signatures of DCIS define biology and correlate with clinical outcomes
BRCA2 linked to inferior outcomes with CDK4/6 inhibitors plus endocrine therapy
Miscellaneous
Olaparib is well tolerated as an additional treatment
Race effects the likelihood to develop lymphoedema following breast cancer treatment
Sentinel lymph node staging is non-inferior to complete axillary lymph node dissection
One in 7 breast cancers detected during screening are overdiagnosed
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