Category: cell press

Correction finally issued seven years after authors promise fix ‘as soon as possible’

A journal has finally issued a correction following a seven-year-old exchange on PubPeer in which the authors promised to fix issues “as soon as possible.” But after following up with the authors and the journal, it’s still not clear where the delay occurred.

Neuron published the paper, “Common DISC1 Polymorphisms Disrupt Wnt/GSK3β Signaling and Brain Development,” in 2011. It has been cited 101 times, 28 of which came after concerns were first raised, according to Clarivate’s Web of Science. 

It first appeared on PubPeer in April 2018, when commenter Epipactis voethii first pointed out figures 2 and 3 of the paper had potential image duplication. 

Continue reading Correction finally issued seven years after authors promise fix ‘as soon as possible’

ICYMI: Second paper by Nobel laureate Thomas Südhof retracted

Thomas Südhof

A 2017 paper coauthored by Nobel laureate Thomas Südhof has been retracted. 

The article, “Conditional Deletion of All Neurexins Defines Diversity of Essential Synaptic Organizer Functions for Neurexins,” was published in Neuron in May 2017 and has been cited 145 times, according to Clarivate’s Web of Science. 

The retraction notice, issued February 11, states:

We, the authors of this publication, have decided to retract the paper because we found that the images in Figure 1D and Figure S4B contain aberrations that cannot be explained, and the original data for these figures are missing. Raw data for the other components of the paper are available, and their reanalysis confirmed the conclusions of the paper. We would like to thank M. Schrag for bringing these image aberrations to our attention.

Continue reading ICYMI: Second paper by Nobel laureate Thomas Südhof retracted

When failure to correct a flawed paper could put patients’ lives at risk

Robert Speth

On April 15, 2021, as COVID-19 was waning several months prior to the surge in deaths associated with arrival of the Delta variant, the journal Cell published an eye-catching paper. 

Titled “Soluble ACE2-mediated cell entry of SARS-CoV-2 via interaction with proteins related to the renin-angiotensin system,” the article stood in stark contrast to the contemporary understanding of the mechanism of SARS-CoV-2 infection, which until then held that ACE2 on the membranes of susceptible cells served as the “receptor” for the virus.

The paper was notable because it claimed that vasopressin, also known as antidiuretic hormone, worsened COVID-19 infections. Vasopressin is known for its ability to promote water retention in the kidneys as well as to constrict blood vessels, but had not previously been associated with COVID-19 infections. 

Upon reading the paper, one of us (MB) noted a large number of inaccuracies. The authors had used the wrong reagent: a high molecular weight precursor of vasopressin rather than vasopressin itself. They also incorrectly portrayed ACE2, the V1B vasopressin receptor, and the AT1 angiotensin II receptor – the primary mediators of their hypothetical mechanism of COVID-19 infection. (PubPeer commenters also pointed out problems in the paper, including a failure of the authors to post their original data.)

Continue reading When failure to correct a flawed paper could put patients’ lives at risk

Software error grounds pigeon-smarts paper

Source

Pigeons definitely get a bad rap. Some might consider them mere rats with wings, purveyors of pestilence, distributors of dung, but rock doves aren’t, well, as dumb as their name might suggest. Pigeons are perhaps the world’s most accurate homers, they seem to have an innate knack for game theory and they can detect breast cancer in mammograms better than many doctors. 

So when researchers in Germany reported in 2017 that pigeons were as adept, if not better, than people in multitasking, the findings seemed plausible. The study, which appeared in Current Biology, garnered a bit of media attention, including this piece in The Scientist, and has been cited five times, according to Clarivate Analytics Web of Science.

Turns out, that was a flight of fancy.

Continue reading Software error grounds pigeon-smarts paper

How a typo in a catalog number led to the correction of a scientific paper — and what we can learn from that

Anita Bandrowski

Papers are corrected for lots of different reasons. In this guest post, Anita Bandrowski, who leads an initiative designed to help researchers identify their reagents correctly, describes one unusual reason for a correction — and explains what researchers can learn from the episode.

Last December, Tianyi Wang and her colleagues published a very interesting paper in Cell Metabolism on the potential link between a gene called JAK/STAT3 and breast cancer. It turns out that breast cancers become resistant to chemotherapy via a pathway that involves JAK/STAT3, and blocking this pathway can re-sensitize the tumor to chemotherapy.

But six months later, they corrected the paper — because of typos in the catalog numbers they’d used. Continue reading How a typo in a catalog number led to the correction of a scientific paper — and what we can learn from that

Caught Our Notice: A team from Harvard, Cornell, Cambridge, HHMI, and UCSF can’t reproduce a paper’s findings

What Caught Our Attention: Any time there’s an issue with a paper co-authored by researchers from such high-profile institutions as Harvard, Cornell, and the University of Cambridge, we take notice. In this case, the group — which included Laurie Glimcher, then-dean at Cornell, now president of the Dana-Farber Cancer Institute — chose to retract a 2013 paper from a Cell journal after learning they couldn’t reproduce some of the experiments. Continue reading Caught Our Notice: A team from Harvard, Cornell, Cambridge, HHMI, and UCSF can’t reproduce a paper’s findings

Delays, arguing over upcoming Cell retraction leave first author “devastated”

After being “blindsided” a few months ago when she was told one of her 2005 papers was going to be retracted, a researcher scrambled to get information about why. And when she didn’t like the answers, she took to PubPeer.

Eight days ago, Shalon (Babbitt) Ledbetter, the first author of the 2005 paper published in Cell, posted a comment on the site announcing the paper was going to be retracted after the last author’s institution, Saint Louis University (SLU), determined that some figures had been manipulated by the last author, Dorota Skowrya. A letter dated September 2, 2015 sent by SLU to Cell describes the results of the investigation — namely, that the manipulations were “cosmetic,” and had no effect on the data or the conclusions. More than two years later, Ledbetter learned the journal was planning to retract the paper, and an initial draft of the notice wouldn’t identify who was responsible; she has since been pulled into a confusing web of blame-shifting and conflicting information that has been, in her words, “heartbreaking.”

Ledbetter wrote on PubPeer:

Continue reading Delays, arguing over upcoming Cell retraction leave first author “devastated”

Researcher at Japan stem cell institute falsified nearly all images in 2017 paper

Shinya Yamanaka

An investigation by Kyoto University in Japan has found a researcher guilty of falsifying all but one of the figures in a 2017 stem cell paper.

Yesterday, Kyoto University announced that the paper’s first author, Kohei Yamamizu, had fabricated and falsified data in the Stem Cell Reports paper. According to the investigation report, none of the other authors were involved in the data manipulation.

Yamamizu works at the Center for iPS cell Research and Application (CiRA) at Kyoto University, directed by Shinya Yamanaka, a Nobel Prize winner for his pioneering work in stem cell biology.

A spokesperson for the journal told us that the authors disclosed the problems last week and Stem Cell Reports will be retracting the paper, published last February.

In the university’s official statement, Yamanaka said: Continue reading Researcher at Japan stem cell institute falsified nearly all images in 2017 paper

Genetic disorder gets name change, but patient’s father still not happy

Credit: Online Mendelian Inheritance in Man

The leading genetic disease database has chosen a new name for a genetic condition, following complaints from a man whose son has the condition.

On Aug. 11, 2017, two days after our coverage of the situation, the Online Mendelian Inheritance in Man (OMIM) database changed the primary name of the phenotype associated with mutations in the RPS23 gene. The new name describes a set of features: “Brachycephaly, Trichomegaly, and Developmental Delay,” or BTDD.

Brachycephaly describes a condition where the back of the head is abnormally flat and trichomegaly refers to extra length, curling, pigmentation, or thickness of the eyelashes.

Marc Pieterse, of the Netherlands, has a son with the rare RPS23 mutation, one of two known patients in the world. The mutation affects ribosomes, cell components involved in protein production. On Aug. 9, we reported on Pieterse’s crusade against OMIM’s original name for the condition, which dubbed it a syndrome. He has feared that calling it a syndrome would “stigmatize” his son’s condition and tried to get the paper underpinning the OMIM entry retracted. The American Journal of Human Genetics has said it will not retract the paper.

Continue reading Genetic disorder gets name change, but patient’s father still not happy

Fearing “stigmatization,” patient’s father seeks retraction of paper on rare genetic mutation

The father of a boy with a rare genetic mutation has accused a scientist of exploiting his child by proclaiming the defect a “genetic syndrome” and naming it after herself.

At an impasse with scientists investigating, publicizing, and interpreting his son’s condition, the father seems willing to use any leverage he can muster to remove the “syndrome” entry in an online genetic disease database. Based solely on an email he obtained from the database director, the father became convinced that if the paper underpinning the entry were retracted, the syndrome would go down with it. So earlier this year, he withdrew his consent and asked the journal that published the paper for a retraction, based on improper patient consent. He has also threatened to lob accusations of research misconduct at the paper’s last author. Continue reading Fearing “stigmatization,” patient’s father seeks retraction of paper on rare genetic mutation