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Biomedical subjects

Wentao Yu

Publications and source records attributed to Wentao Yu.

6 recordsLinked to original sources

Translational control by RPL22L1-specific ribosomes enhances DNA repair and chemoresistance.

Ribosome heterogeneity has emerged as a regulatory layer in gene expression, yet its biological roles in cancers remain poorly characterized. Here, we identify RPL22L1, a paralog of the ribosomal protein RPL22, as a key modulator of DNA damage response (DDR) in colorectal cancer cells. DNA damage induces RPL22L1 upregulation and ribosomal incorporation, forming RPL22L1-specific ribosomes. Ribosome profiling reveals that RPL22L1-containing ribosomes preferentially translate mRNAs with highly structured 5' untranslated region (5'UTR). In particular, RPL22L1 enhances the translation of ATRX through a cap-independent mechanism. ATRX subsequently recruits DNA-PKcs to DNA damage sites, thereby enhancing the DNA repair capacity. RPL22L1 loss creates exploitable DDR vulnerabilities, sensitizing cancer cells to cisplatin and PARP inhibitors in vitro and in vivo. Collectively, these findings uncover a specialized ribosome-mediated translational program in DDR and highlight RPL22L1 as a potential therapeutic target in DDR-based cancer therapy.

DNA Repair↗

4,5-propylenedithio-1,3-dithiole-2-thione and 4,5-propylenedithio-1,3-dithiol-2-one.

4,5-Propylenedithio-1,3-dithiole-2-thione, C(6)H(6)S(5), (I), crystallizes in the centrosymmetric space group P2(1)/c. The molecular packing is characterized by pairs of S.S intermolecular contacts between neighbouring molecules, which may account for the rather high thermal stability of the crystal. 4,5-Propylenedithio-1,3-dithiol-2-one, C(6)H(6)OS(4), (II), in which an O atom replaces the terminal S atom of (I), crystallizes in the non-centrosymmetric polar space group Cc. The packing pattern of (II) indicates that the macropolarization direction is along [101]. Although the packing patterns are qualitatively significantly different, the molecular structures of (I) and (II) are similar, each exhibiting a chair conformation.

Journal Article↗

Formation of a novel 1D supramolecule [HgCl2(ptz)]2.HgCl2 (ptz = phenothiazine): a new precursor to submicrometer Hg2Cl2 rods.

A novel supramolecule [HgCl(2)(ptz)](2).HgCl(2) (ptz = phenothiazine) with uncoordinated inorganic salt HgCl(2) presented in a 1D chain was first prepared and then successfully applied as a new precursor in the preparation of submicrometer Hg(2)Cl(2) rods. Single crystal X-ray analysis showed that the 1D chain structure is stabilized by hydrogen bonds between adjacent chains and the coordination mode of the ligand phenothiazine is unusual with large steric inhibition other than the chain directions. The results revealed that the particular chain structure plays a significant role in the formation of the Hg(2)Cl(2) rods.

Journal Article↗

N-ethylpyridinium bis(2-thioxo-1,3-dithiole-4,5-dithiolato)nickelate.

The title compound, (C(7)H(10)N)[Ni(C(3)S(5))(2)] or (Etpy)[Ni(dmit)(2)] (where Etpy is the N-ethylpyridinium cation, C(7)H(10)N(+), and dmit is the 2-thioxo-1,3-dithiole-4,5-dithiolate dianion, C(3)S(5)(2-)), crystallizes in the P-1 space group with two molecules in the asymmetric unit. The [Ni(dmit)(2)](-) monoanion has a planar D(2h) conformation, with the central Ni atom and the four coordinated S atoms forming an NiS(4) square plane. The six-membered ring of the Etpy cation also shows good planarity, as expected. There are two main types of disorder in the two Etpy cations. Several short intermolecular interactions are present, such as S...S, Ni...S and Ni...Ni, which help to form the enhanced three-dimensional structure of the crystal.

Journal Article↗

2'-Hydroxy-4"-dimethylaminochalcone.

The title compound, 3-[4-(dimethylamino)phenyl]-1-(2-hydroxyphenyl)prop-2-en-1-one, C(17)H(17)NO(2), is a chalcone derivative substituted by 2'-hydroxyl and 4"-dimethylamino groups. The crystal structure indicates that the aniline and hydroxyphenyl groups are nearly coplanar, with a dihedral angle of 10.32 (16) degrees between their phenyl rings. The molecular planarity of this substituted chalcone is strongly affected by the 2'-hydroxyl group.

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Tetra-n-butylammonium bis(2-thioxo-1,3-dithiole-4,5-dithiolato-kappa2S4,S5)nickelate(III).

The crystal structure of the title compound, (C(16)H(36)N)[Ni(C(3)S(5))(2)], is isomorphous with that of the corresponding Pt complex but different from the structures reported for compounds of the same chemical composition, and so provides a new crystalline phase of this complex. The nickel complex anion has good planarity and lies on a crystallographic inversion centre. There is disorder in the two terminal C atoms of two of the butyl chains of the tetra-n-butylammonium cation, the N atom of which is located on a twofold axis.

Journal Article↗