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It is official now! 🥳
Our latest. Led by the very talented @aHoi_Ching
Cell cycle dysregulation of globally important SAR11 bacteria resulting from environmental perturbation nature.com/articles/s41564-0…
ChuánKǎi Chéng 程傳凱 retweeted
Strong agreement in absolute marine prokaryote abundance from epifluorescence microscopy and internal-standard-corrected metagenomics @USC_MEB academic.oup.com/ismecommun/…
ChuánKǎi Chéng 程傳凱 retweeted
Congratulations 👏to PriME members Hagen Buck-Wiese and Naomi Levine on this publication, in which they call for moving beyond “optimal” phenotypes measured under fixed conditions to capture microbial plasticity in a changing ocean. 🌊🦠
Life out of equilibrium: Rethinking how we quantify & model marine microbial phenotypes
Forum examines marine microbial physiology,arguing for quantification of phenotypic plasticity to ID strategies across environments ¶meterize biogeochemical models
cell.com/cell-host-microbe/a…
ChuánKǎi Chéng 程傳凱 retweeted
Rethinking the origin of life at seafloor hydrothermal vents pnas.org/doi/10.1073/pnas.26…
ChuánKǎi Chéng 程傳凱 retweeted
We really enjoyed this talk, with more than 20 researchers from across Japan joining us! We will continue to create opportunities like this for researchers in Japan to connect and discuss with scientists conducting cutting-edge microbial research around the world.
統合微生物科学研究会(IMS)のオンラインセミナー開催のお知らせです。
8/28 10:00(JST)〜、UCLAのChuankai Cheng氏が、今年Nature Microbiologyに発表したSAR11の生理・進化的トレードオフに関連する内容を話してくれます。
nature.com/articles/s41564-0…
参加登録は、
oist.zoom.us/meeting/registe…
ChuánKǎi Chéng 程傳凱 retweeted
If you're interested in subscribing seminar information about any microbial sciences across Japan, feel free to register yourself through the link.
docs.google.com/forms/d/e/1F…
ChuánKǎi Chéng 程傳凱 retweeted
Congrats Otto! Another good example of how microbial interactions drive biogeochemical cycling!
Excited to share our latest paper in @Nature, featuring the fantastic work of Andi Sichert. A systems ecology approach to understanding how microbial communities digest complex carbohydrates in the ocean:
nature.com/articles/s41586-0…
ChuánKǎi Chéng 程傳凱 retweeted
Meet our lab!! instagram.com/p/Db_mIRhEppb/…
ChuánKǎi Chéng 程傳凱 retweeted
Recombitrons enable bacterial genome editing across phyla nature.com/articles/s41564-0…
ChuánKǎi Chéng 程傳凱 retweeted
The history of enzyme evolution embedded in metabolism pnas.org/doi/abs/10.1073/pna…
ChuánKǎi Chéng 程傳凱 retweeted
Excited to share our new Comment in @NatureComms:
We join the discussion on the terminology of synthetic microbial communities and propose that SynComs should be more rigorously defined rather than simply renamed.
nature.com/articles/s41467-0…
ChuánKǎi Chéng 程傳凱 retweeted
Predictable shifts in microbial species composition lead to community-wide robustness to environmental stress nature.com/articles/s41564-0…
ChuánKǎi Chéng 程傳凱 retweeted
Multi-omic data fusion reveals the in vivo enzyme kinetics of Vibrio natriegens at the genome-scale biorxiv.org/content/10.64898…
ChuánKǎi Chéng 程傳凱 retweeted
#ASCO26
This one is special.
This is the hottest paper of 2026 and potentially in the history of pancreatic cancer.
Let’s dive in.
RASolute 302: Daraxonrasib vs investigator’s choice chemotherapy in previously treated metastatic pancreatic cancer
Abstract LBA5 (soon!)
Presentation: May 31, 2026, 3:21-3:33 PM CDT
For decades, pancreatic cancer has been where good ideas go to die.
We have optimized chemotherapy. We have sequenced chemotherapy. We have celebrated modest gains.
But the central driver of PDAC has always been sitting there in plain sight:
RAS.
More than 90% of pancreatic cancers have oncogenic RAS mutations, and until recently, we had essentially nothing direct to do about it.
Daraxonrasib is an oral RAS(ON) multiselective inhibitor targeting the active GTP-bound state of mutant and wild-type RAS.
And in RASolute 302, it delivered.
Quick hits:
📌 Phase 3 international randomized trial 500 patients with previously treated mPDAC Daraxonrasib vs investigator’s choice chemotherapy
🧬 RAS G12 population
91.8% of patients had RAS G12 mutations
📈 OS in RAS G12 population
13.2 vs 6.6 months
HR 0.40
P<0.001
📈 OS in overall population
13.2 vs 6.7 months
HR 0.40
P<0.001
📊 PFS in RAS G12 population
7.3 vs 3.5 months
HR 0.45
P<0.001
📊 PFS in overall population
7.2 vs 3.6 months
HR 0.49
P<0.001
🔥 12-month OS
Overall population: 53.2% vs 17.3%
⚠️ Toxicity matters, but this was not just more efficacy for more toxicity
Grade ≥3 AEs: 61.8% vs 69.6%
TRAEs leading to discontinuation: 1.2% vs 11.2%
This is the kind of survival curve we almost never get to see in pancreatic cancer.
This validates RAS(ON) inhibition in the most RAS-addicted major cancer. It takes a target we have talked about for decades and turns it into a clinically meaningful survival benefit in a randomized phase 3 trial.
The next questions come fast: 1L combinations, maintenance, perioperative disease, sequencing, resistance, toxicity management, and whether this becomes a new backbone.
RAS is here, and it couldn’t have come sooner.
nejm.org/doi/full/10.1056/NE…
@TheGutonclab @UGrewalMD @TimothyJBrownMD @OncoAlert @Onco_Nexus @ASCO
@NazliDizman @LauraAlderMD @DVAraujoMD @DrBarbiOnc @LauraEsfeller @FunchainMD @YGaritaonaindia @DrSAHaddad @jgong15 @iandresmeraz @SakditadMD @RamilaShilpakar @RohitBanwar @lungoncdoc
ChuánKǎi Chéng 程傳凱 retweeted
people aren’t celebrating this pancreatic cancer breakthrough enough. it should be international news
ChuánKǎi Chéng 程傳凱 retweeted
❓Can we predict ocean carbon cycling by looking at what microbes do rather than who they are?🌊
During his PhD in PriME, Ryan Reynolds explored this question by combining global metagenomic with metabolic modeling 😀
Check out his last publication 👇
science.org/doi/10.1126/scia…
ChuánKǎi Chéng 程傳凱 retweeted
Marine microbiomes and their expanding role in biotechnological potential: a systematic review link.springer.com/article/10…
ChuánKǎi Chéng 程傳凱 retweeted
Why do some cells produce more protein than others? Jasmine Tat (UCSD & Amgen) conducted a detailed study into the single-cell transcriptome, while measuring mAb production in single cells too with SEC-seq. Check out the preprint! doi.org/10.64898/2026.04.14.…
















